4G Clinical is a global leader in randomization and trial supply management (RTSM) and clinical supply optimization software for the life sciences industry. Our RTSM solutions bring flexibility and efficiency to clinical trials while offering exceptional quality and performance. The complexity of today’s trials is inadequately supported by traditional IRT and supply optimization systems. Our solutions utilize Natural Language Processing (NLP) to enable truly flexible clinical trials. This ensures more time can be spent on running your trials to ultimately bring crucial medicines to patients faster.
4G Clinical
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August Research is a boutique CRO managing Phase I-IV clinical trials across Europe. The company is focused around Clinical Operations and Pharmacovigilance, with a high-touch approach to site management, resulting in better quality and higher enrollment. The company management team has been working together for nearly 20 years and has deep expertise in Central and Eastern Europe. Clinical services include all Regulatory/EC submissions, study start-up, site contracting, monitoring, project management, and quality assurance/audits. On the PV side, August Research provides full drug safety management services including safety plans, database management, case entry, and reporting. Contact us to learn how August Research can manage your trials for success in Europe.
August Research
Since 1975, ACM Global Laboratories has been a recognised leader in global clinical trial testing services. Through wholly-owned facilities and partner laboratories, we support clinical trials in more than 65 countries around the globe. Our full-time staff of laboratory experts span all medical disciplines including central lab services, pathology, microbiology, toxicology and more…
ACM Global Laboratories
APICES is a full-service CRO with offices in Spain and France and capabilities to cover all Western European countries. APICES has deep experience in oncology, hematology, and all other therapeutic areas and provides a wide range of clinical research and development services, from project design to publication of results. Flexibility, Excellence and Client Satisfaction are our key drivers since 2009 proven with > 50 public acknowledgements in scientific journals to date.
APICES
Aixial Group is a leader in CRO services with expertise in oncology, cell & gene, and rare disease therapies that spans the entire development of pharmaceuticals, biologics, and devices. With more than 1,000 employees worldwide, Aixial provides expertise and a wide range of solutions, including full-service, FSP, and consulting.
Aixial Group
Axiom is celebrating over 22 years of delivering hundreds of studies in dozens of countries. Since its founding in 2001, Axiom has delivered data-driven, powerful, and cost-effective eClinical Solutions and Services dedicated to small-to-medium life science companies. Axiom Fusion eClinical Suite is the most adaptable, Unified Platform that serves as the Connected Hub for all your Clinical Trial and operational data and reporting. Choose from 15+ unified modules on a single platform: EDC, DM, RTSM/IRT, CTMS, Inventory Management, ePRO, eConsent, Patient Portal, AE/SAE Tracking, Safety Database, Central/Local Lab, Imaging Management, eTMF, and 24/7 Project and Clinical Data Reporting. We are an embedded partner dedicated to the success of your study, offering managed services such as: Data Management, On-Demand Data Analytics, Biostatistics, Clinical Management, eTMF Management and Pharmacovigilance.
Axiom Real-Time Metrics
Ancillare fully manages, medically advised ancillary supply and equipment programs for global Phase I-IV clinical research with corporate offices in the US and the Netherlands, and distribution hubs in Argentina, Australia, Brazil, Canada, China, India, Israel, Japan, Korea, Mexico, Philippines, Taiwan, Turkey, and United Kingdom.
Ancillare
Alderley Analytical is a Contract Research Organisation (CRO) specialising in Regulatory Bioanalysis. Our GLP and GCP accredited laboratories specialise in analysing plasma, blood, urine, or other tissue samples to detect and quantify the drug or biomarker in the sample, for your pharmacokinetic, exposure and biomarker endpoints. Whether your drug is a small molecule, peptide, oligonucleotide or large molecule we have the technology and expertise to support your project.
Alderley Analytical
Acolad Life Sciences is the business unit of Acolad that specializes in certified language solutions for Pharma, Medical devices, Medtech and Clinical Research Organizations. Supported by the unmatched expertise of its medical translators and technology-driven language solutions, Acolad Life Sciences partners with its clients through every stage of product development - from clinical trials to post-market surveillance - acting in compliance with industry best practices and regulatory requirements of national and international health authorities worldwide.
Acolad Life Sciences
Judi by AG Mednet is the award-winning clinical trial collaboration platform that streamlines workflows and accelerates the process of developing therapies for patients across the world. Trusted by 19 of the top 20 global biopharmaceutical sponsors and 5 of the top 6 global CROs, Judi has delivered over 2500 studies across 170 countries and 71,000 sites to support clinical event and endpoint adjudication, central eligibility review, data safety monitoring boards, medical imaging, and other mission-critical areas of clinical development.
Judi by AG Mednet
Almac Clinical Services have been partnering with clients for 30+ years, we set the standard for developing effective supply chain strategies that ensures our sponsors can overcome their unique challenges and deliver supply continuity to patients wherever they are in the world.
We have a range of tools and services to help you achieve this, from forecasting/inventory management, supply chain strategy to global logistics management, end-to-end temperature solutions, IRT set-up and strategy, direct to patient distribution and pharmacy services alongside our clinical packaging and labelling facilities.
When you partner with Almac you are partnering with experts who Supply With CareTM
Almac
A2 Healthcare (A2) is a Japan-Taiwan industry leading clinical CRO with more than 1,300 employees. A2 have opened its new US office in Boston area in 2023. A2 is the expert for clinical development in Japan and Taiwan and are interested to support US pharma/biotech to reach out to its region. Also have a unique program to invest in their pipeline, especially for drugs which are already marketed or under development in US.
A2 Healthcare
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Biopharma Group
Biopharma Group’s highly experienced team provides comprehensive CDMO services from R&D and consultancy solutions for lyo and liquid formulations to fill-finish GMP clinical manufacturing (phase 1 & 2) to the pharmaceutical, diagnostic and biotech industries.
BioBridges
PharmAlliance engages biotech sponsors and CROs with fully vetted contract pros as follows:
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* BioBridges: Commissions nine functional areas of fractional (full and part-time) clinical trial research professionals.
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* Monitor-For-Hire: Provides 4000+ seasoned and fully vetted global CRAs for our partners who seek efficiency and readiness in clinical monitoring.
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* CHEORS: Conducts Cutting-edge health economic insights, economic modeling, country adaptations of the economic models for HTA submissions, systematic literature review,
meta-analysis, and database analysis. Ultimately assisting pharmaceutical companies with
market-access planning and support in payers to modify economic models for evaluating
value-based contracts.
BRANY
The Biomedical Research Alliance of New York (BRANY) is a national organization providing support services to sponsors, CRO's and investigators involved in research in a wide variety of therapeutic areas, medical devices, biologic and diagnostic trials. Staffed by multi-disciplinary experts, BRANY is an expedited "end-to-end solution"​ for clinical trials. BRANY is able to offer its partners a turnkey solution for expedited site identification and study start-up (SMART-Start-60), Central IRB Services, IBC services, Medicare Coverage Analysis Services, Research Education, and Quality Assurance auditing and consulting services. BRANY was founded in 1998 by nationally-ranked academic medical centers, which today includes: NYU School of Medicine, Montefiore Medical Center, Mount Sinai School of Medicine, and North Shore-Long Island Jewish Health System.
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Clinical Services International (CSI) provides the most comprehensive solutions to clinical trial supplies including sourcing of medicines and devices, distribution and all services needed for successful conduct of studies.
We have offered our solution to more than 1000 clinical trials all over the world.
Headquartered in London and with operations in 5 continents, we provide efficient solutions to the most complex adaptive trials worldwide.
We accelerate drug development and reduce timelines by providing a fully integrated service.
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Address Regulatory, Quality, Operational, Clinical Requirements, and Forecasting
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Manage the entire supply chain and offer tailor-made solutions
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Comprehensive expertise in Oncology and Biosimilar products
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Direct access to all major Pharmaceutical Manufacturers and more than 95 audited suppliers globally.
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Trusted partner of leading Biopharmaceuticals, CROs and CMOs.
Clinical Services International
CRYOPDP is a global expert in temperature-controlled logistics and supply chain solutions, dedicated to the clinical trial and cell & gene therapy communities, that aims to improve the health of people around the world. Truly focused on the customer and patient needs, CRYOPDP, through a dedicated team, plans, manages, and implements a tailor-made solution to fit our customer's business goals.
Cryoport
Colibri Scientific
A clinical trial is only as good as the quality of its samples!
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Colibri Scientific’s fast and flexible sample operational services focus on ensuring that every sample generates a valid result for your study. Our approach allows the clinical team to focus on patient safety and recruitment, while Colibri ensure that your samples are top priority.
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All our services are designed to minimise error across the sample lifecycle. From bespoke visit kits through sample logistics and tracking to bioanalysis management, our sample experts deliver a service second to none. Flexibility is in our DNA!
Catalent solves today’s clinical trial challenges and develops innovative solutions for the future. Catalent’s commitment to quality and service excellence is evident in its comprehensive and flexible solutions for small molecules, biologics and cell and gene therapies. With modern global facilities, and 25+ years’ experience reliably supplying thousands of studies of all sizes and complexities around the world, services include:
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Clinical supply management
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Integrated formulation development, clinical manufacturing & blinding
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Specialty handling (potent, cytotoxic, controlled)
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Direct comparator/reference product sourcing
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Clinical packaging/labeling
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Extensive clinical storage, cold chain capabilities & global distribution
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Demand-led supply
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Direct-to-patient solutions
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Clinical returns, reconciliation & destruction
Catalent Clinical Supply
Clinicology is a bespoke CRO for Phase I-IV CTIMP and medical device studies. Our advantages are our speed and flexibility, with rapid project startup and team deployment with our network across Europe and the US. Our core services include site startup, monitoring, project management, regulatory submissions and patient recruitment.
Clinicology
​Comac Medical is a boutique CRO and SMO with a global footprint that renders the full spectrum of clinical trial services Phase I - IV in more than 30 countries across Europe, North America, and Asia. Our experienced team provides personalized support at every stage of the clinical trial process
Comac Medical
CRIO revolutionizes clinical research with cutting-edge cloud technology. CRIO enables remote monitoring and instant data review with CRIO Reviewer, an integrated eSource/EDC solution. Capturing data in real-time and ensuring compliance with various regulations, including 21 CFR 11, ICH-GCP, GDPR, and HIPAA, CRIO eliminates redundant data entry and safeguards data integrity.
CRIO
Clinicology is a bespoke CRO for Phase I-IV CTIMP and medical device studies. Our advantages are our speed and flexibility, with rapid project startup and team deployment with our network across Europe and the US. Our core services include site startup, monitoring, project management, regulatory submissions and patient recruitment.
Clinicology
90% of all biotech companies spend >300 hours/study comparing vendors and grappling with excel files.
How do you select vendors for a new clinical trial? Using Excel Files? Does that allow for 1:1 comparison?
What if there is a platform that can help
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create, send and receive proposals on the cloud and
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provide you with AI-based analytics to compare, negotiate and find the best vendor both in terms of price and quality.
That is what Clin.AI can do for you.
Once you select vendors, the Clin.AI platform also helps you manage vendors (change Orders, etc) and never let your studies go off track.
Save hours of frustration, get 8 weeks faster to FPI and save thousands of dollars in the process.
Clin.AI
Clario is a leading healthcare research and technology company that generates high quality clinical evidence for our pharmaceutical, biotech, and medical device partners. We offer comprehensive evidence generation solutions that combine eCOA, cardiac solutions, medical imaging, precision motion, and respiratory endpoints.
Clario
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Delve Heath
Delve Health is a Virtual Research Organization (VRO) founded in 2017 which now has a global presence, we make clinical research faster, easier and more cost effective for our clients, powering clinical trials with a mix of solutions, including IRT/RTSM, electronic consent, patient engagement applications and remotely collect diaries and patient outcomes directly from a patient's connectable device all from the patient's home, school or workplace.
DISTILL is a DIY, Drag & drop EDC, flexible, fully compliant, quick and easy to set-up. All for a very attractive budget.
Great fit for pharmas, biotechs, academia, non-profit. For all phases and TA.
Perfect partner for CROs to complete their EDC offering with a mature product that will match their customers small budget.
DISTILL Technologies
ESMS Global is a niche service provider offering 24/7 emergency medical response services for Clinical Trials and Medical Information.
With global contracts across 80 countries, speaking 45 languages, our background and culture is built on providing support in emergency situations. We focus on patient safety creating a reliable and robust solution for your business.
ESMS Global
Founded in Prague in 2004, EastHORN is today one of the leading CROs in Europe. We operate in over 30 countries in the region with an experienced staff comprised largely of physicians and PhDs. In January 2023 EastHORN joined Novotech, the leading Asia-Pacific centered CRO, as part of Novotech global expansion strategy to provide biotech clients with in-country expertise across Asia-Pacific, North America, and Europe to deliver their global drug development programs.
EastHORN a Novotech Company
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Endpoint Clinical is an interactive response technology (IRT) solutions provider that supports the life sciences industry. Our innovative, high-quality randomization and clinical trial management technologies are backed by over a decade of award-winning experience and expertise. Endpoint is headquartered in Wakefield, MA, with offices across the US, EU, and Asia.
Endpoint
The companies of Eurofins Clinical Trial Solutions provide a seamless solutions-based approach in support of phase I to IV clinical trials with a unique analytical testing portfolio for Central Laboratory Services, Bioanalytical Services and complex Biomarker Assay Development and Testing Services for drug and vaccine development.
Eurofins Clinical Trial Solutions
EMB Statistical Solutions, LLC is a niche contract research organization serving the pharmaceutical and biotechnology industries. EMB specializes in Data Management, SAS programming and Statistical Analysis/Reporting. Formed in 2000, EMB has had near perfect retention, is associate owned, and has a proven track record of success. EMB uses a team approach that functions as a seamless partner on projects. Each team member is an expert in their field with an average 20+ years of experience. EMB is Powered by Experience.
EMB Statistical Solutions
Everest Clinical Research
​Everest Clinical Research is a full-service, global CRO managing trials end-to-end—from study feasibility and project management to database lock and final study reports. Everest has deep clinical experience in more than 30 therapeutic areas with extensive expertise in oncology, CNS, infectious and rare diseases. The company insists on operational excellence, providing clients with personalized, flexible and detail-oriented attention—illustrated through its high referral rate. Nearly 98% of its clients are recommended from other satisfied customers.
Since its inception as a biostats and statistical programming center of excellence, Everest has grown every year—recently celebrating its 20th anniversary. Today the company serves more than 100 active clients worldwide from its offices in North America, Europe and Asia.
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FyoniBio offers customized assay development and clinical sample analysis under GCLP. Our focus are PK, ADA, NAb, biomarker and potency assays, its development and validation for clinical development of therapeutic oligonucleotides, peptides and proteins. Additionally, FyoniBio is the ideal partner for development of biotherapeutics with our innovative CHOnamite® / GlycoExpress® technologies.
Fyoni Bio
Fortrea is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with small/mid-size biotech and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology enabled trial solutions and post-approval services.
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Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team of more than 19,000 people working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally.
Fortrea
Florence Healthcare is a leading provider of Site Enablement solutions that streamline clinical research operations and improve collaboration among research sites, sponsors, and CROs. With a focus on driving innovation and enhancing the trial site experience through site enablement, Florence Healthcare is committed to closing the cure acceleration gap and revolutionizing the clinical trial industry.
Florence Healthcare
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Glatt Pharmaceutical Services: Your full-service partner in drug development and manufacturing. With cutting-edge technologies and a holistic approach, we streamline processes from concept to commercialization. Trust us for precise solutions, ensuring efficacy, safety, and quality at every step. Your success, our commitment.
Glatt Pharmaceutical Services
GEOSTORAGE LTD is a fully licensed GDP and ISO compliant pharmaceutical supplier with own Courier , storage, and distribution services during the Clinical Trial , that was founded in 2010. Our strength lies in our qualified personnel, experienced wide range of services, we strictly follow GMP/GDP and ISO requirements to ensure patient safety. For us maintaining a good reputation for safety and reliability is of utmost importance.
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Trust and save your time!
GeoStorage
G&L Healthcare Advisors is evolving rapidly to become a trusted leader in biopharmaceutical solutions.
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With decades of experience in regulatory and quality services, we leverage our global expertise and advanced technologies to provide innovative solutions for the pharmaceutical, biopharmaceutical, and biotechnology industries.
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From drug development to market access, our unified, best-in-class solutions are here to drive your success across the entire product lifecycle.
G&L Healthcare Advisors
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​HeartcoR Solutions (HCS) is a leading Cardiac Safety Core Lab serving the Medical Device and Pharmaceutical Industries. HeartcoR has conducted 32 global IDE-PMA study projects since 2018 and has extensive understanding of Cardiac Safety execution to yield high study subject compliance in support of regulatory submissions. HCS’ also serves Bio-Pharmaceutical companies conducting intensive QT and phase I-IV safety studies. The Company’s 50 employees hold a required certifications and our Electrophysiologist/Cardiologist analysis team are recognized experts in heart rhythm analysis. HeartcoR is based in Schaumburg Illinois, twenty minutes north of O’Hare Airport.
HeartcoR Solutions
Harbor Clinical is a women-owned clinical research services firm with headquarters in the Boston biotech area. As a Functional Service Provider (FSP) offering Staff Augmentation, Consulting, and Single-Service resourcing models, Harbor Clinical's core competencies include:
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Quality Assurance (Inspection Readiness, site/vendor audits, etc)
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Vendor Oversight
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Clinical Operations
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Data Management
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Programming
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Biostatistics
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Medical and Safety Management
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Medical Writing
Harbor Clinical
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H1 harnesses and democratizes access to hard-to-assemble HCP information, claims data, ground-breaking research, and expert opinions. H1’s ability to gather and make sense of billions of data points and deliver them in workflow-friendly solutions helps to accelerate the development, launch, and dissemination of life-saving treatments; drive meaningful engagements with key opinion leaders; and help ensure equitable access to healthcare services.
H1
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Illingworth Research Group provides mobile research nursing and patient concierge services supporting patient enrollment and retention in decentralized trials. We are the longest established mobile home nursing provider with 20+ years of experience, offering our services in over 45 countries globally. Illingworth brings the patient to the trial and the trial to the patient.
Illingworth
IDDI is an expert clinical data services &
high-level strategic consulting CRO, providing biometry clinical trial services for pharmaceutical, biotechnology, and medical device/diagnostic companies.
Since 1991, IDDI offers the medical expertise, biostatistical acumen and profound knowledge of the regulatory environment that are required to design and launch clinical trials.
IDDI
Intelsius has been designing and manufacturing environmentally sustainable and regulatory compliant sample transport and temperature-controlled packaging for 25 years.
As well as offering a diverse range of sample transport and temperature-controlled packaging solutions, our expert Technical Services team and ISTA-certified laboratory ensure we can design, test and qualify your packaging with your specific payload and shipping lane in mind.
Intelsius
At IOMED we develop AI-powered technology for healthcare data activation. Our Natural Language Processing system is capable of standardizing both structured and unstructured healthcare data, leaving it ready to be leveraged for secondary purposes. By doing so, we pave the way for a global, data-driven healthcare ecosystem.
IOMED
IQVIA Biotech delivers flexible clinical solutions designed to help biotech and emerging biopharma companies get treatments to patients. Our clinical development team brings expertise from two decades of planning and executing clinical trials exclusively for biotech companies. Drawing on IQVIA's unparalleled data and advanced analytics, IQVIA Biotech creates intelligent connections to deliver powerful insights to help customers accelerate clinical development of innovative medical treatments.
IQVIA Biotech
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ICON is the world's leading clinical research organisation, powered by healthcare intelligence. From molecule to medicine, we advance clinical research providing outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We develop new innovations, drive emerging therapies forward and improve patient lives.
ICON
We help pharmaceutical companies and healthcare professionals access treatment for patients in need worldwide.
As a specialized service partner with expert teams across the globe we:
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Provide global comparator sourcing solutions and services for clinical trials
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Facilitate early access and unlicensed medicines programs
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Distribute licensed medicines worldwide
Inceptua
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Clinical Services International
Clinical Services International (CSI) provides the most comprehensive solutions to clinical trial supplies including sourcing of medicines and devices, distribution and all services needed for successful conduct of studies.
We have offered our solution to more than 1000 clinical trials all over the world.
Headquartered in London and with operations in 5 continents, we provide efficient solutions to the most complex adaptive trials worldwide.
We accelerate drug development and reduce timelines by providing a fully integrated service.
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Address Regulatory, Quality, Operational, Clinical Requirements, and Forecasting
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Manage the entire supply chain and offer tailor-made solutions
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Comprehensive expertise in Oncology and Biosimilar products
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Direct access to all major Pharmaceutical Manufacturers and more than 95 audited suppliers globally.
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Trusted partner of leading Biopharmaceuticals, CROs and CMOs.
Komtur Pharmaceuticals is a leading specialist in the procurement and distribution of pharmaceutical products – including resources for clinical trials. We’ve built an unparalleled reputation for streamlining pharmaceutical supply chains along the entire product lifecycle, resolving challenges, reducing risks, minimising delays, and cutting overheads.
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Through our integrated global networks of subsidiaries and qualified suppliers, we ensure borderless sourcing, storage and delivery services from anywhere, to anywhere in the world.
Komtur
Keosys Medical Imaging is a central imaging lab providing medical image management and reading services to biotech and pharma clients around the world. Keosys can handle CT, MRI, PET, SPECT and X-ray scans for your clinical trials and has its own team of developers to quickly manage new imaging criteria.
Keosys Medical Imaging
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Lonza
Lonza is a preferred global partner to the pharmaceutical, biotech and nutrition markets. We work to enable a healthier world by supporting our customers to deliver new and innovative medicines that help treat a wide range of diseases. We achieve this by combining technological insight with world-class manufacturing, scientific expertise and process excellence.
Lumis Life Science Consulting GmbH is an independent subsidiary of Lumis International GmbH to provide customer-tailored consulting and solutions for regulatory consulting and Services, clinical trial oversight and vendor management and quality management. Jointly with our customers, we develop tailored solutions to optimise their clinical development program. We collaborate with a network of experienced subject matter experts, cooperation partners, and consultants.
Lumis
Leapcure connects patients with clinical trials to make research more equitable and efficient with patient advocacy at the forefront. Patients are the experts in their condition and advocacy groups provide a platform for patient voices, and Leapcure is expert at discovering them efficiently. Working directly with these communities is the key to pushing research forward in an inclusive way. EQuitable clinical trials are trials where empathy and emotional intelligence are crucial, helping to build trusted connections between sponsors, sites, KOLs, and patients.
Leapcure
Medicover Integrated Clinical Services is a global service and solution provider dedicated to support the Drug Development Industry from Research and Development through Clinical Studies and Commercialization with access to patients and biosamples, advanced diagnostics and central lab services through Medicover Group network of hospitals, clinics and diagnostic laboratories.
Medicover
MLM Medical Labs
MLM Medical Labs is a global leading specialty and central laboratory with comprehensive research services and analytical capabilities in Europe and North America. Offering standard and fully customizable biological specimen testing and auxiliary logistics services across a wide spectrum of therapeutic areas from nonclinical and preclinical through phase IV clinical trials.
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Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. With over 20 years of groundbreaking technological innovation across more than 30,000 trials and 9 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and the largest patient-level historical clinical trial data set in the world. More than 1 million registered users across 2,100+ customers trust Medidata’s seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster. A Dassault Systèmes company (Euronext Paris: FR0014003TT8, DSY.PA), Medidata is headquartered in New York City and has been recognized as a Leader by Everest Group and IDC.
Medidata
Mayet is a clinical trial software, centralising processes, data and communication for robust vendor management an oversight. Our platform saves time on vendor-related tasks, eliminating inefficient processes, collects and presents partnership data for data driven decisions, and provides access to key stakeholders, for communication and reporting.
Mayet
Mednet is a healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Mednet’s comprehensive, EDC-centric eClinical platform improves the efficiency of clinical studies of all types and sizes. Pharmaceutical, medical device, biotechnology and CROs have trusted Mednet for over 21 years to accelerate clinical development.
Mednet
Myonex is a leading global clinical trial supply company with more than 30 years of experience supporting sponsors ranging from Big Pharma to small biotech, as well as CROs, and other service providers. We offer four unique services—sourcing, packaging/labeling, equipment and supplies, and patient solutions—that work together to create flexibility, improve effectiveness, increase efficiency, and eliminate waste. We problem-solve and tailor solutions to the specific requirements and complexities of each trial, and sponsors and CROs benefit from the simplicity of having a single vendor that can provide an optimized, integrated clinical trial supply strategy that saves time and money.
Myonex
At Median, we transform medical images into meaningful, actionable insights to help better diagnose, treat, and monitor patients. Median’s Imaging CRO business provides best-in-class clinical trial imaging solutions for oncology studies, empowering our life sciences partners to accelerate the development and delivery of life-saving cancer treatments with unmatched operational excellence and reliability. And we don’t stop there. We are forging the way when it comes to innovative imaging technology, leveraging the latest in AI-powered imaging intelligence to develop actionable insights for sponsors worldwide.
Median
Clinical trial sponsors should be able to locate independent clinical trial monitors (CRAs) anywhere in the world, FAST. MonitorForHire.com is a patented web-based resourcing tool with over 4,000 registered and pre-qualified monitors in 60 countries including the North American, Latin America, UK, Europe, Asia & MENA.
MonitorForHire.com
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Founded in 1997, Novotech is a global full-service clinical Contract Research Organization (CRO) focused on partnering with biotech companies to accelerate the development of advanced and novel therapeutics at every phase.
Recognized for its industry-leading contributions, Novotech has received numerous prestigious awards, including the CRO Leadership Award 2023, the Asia Pacific Cell & Gene Therapy Clinical Trials Excellence 2023, the Asia-Pacific Contract Research Organization Company of the Year Award since 2006.
The Company offers a comprehensive suite of services including laboratories, Phase I facilities, drug development consulting, regulatory expertise, and has experience with over 5,000 clinical projects, including Phase I to Phase IV clinical trials and bioequivalence studies. With a presence in 34 office locations and a dedicated team of 3,000+ professionals worldwide, Novotech is a trusted end-to-end strategic partner of choice.
Novotech
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O4 Research is a UK/Ireland based provider of innovative, sector leading clinical trial services and ‘On & Off’ site management solutions. For over a decade we have successfully delivered full and functional services for Top 20 Pharma, FMCG and medical device clients across Clinical Phases II-IV and Post Approval/RWE studies.
Four values power our success, Yours, too.
O4 Research
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OPIS was founded in 1998 by medical doctors from the Pharma Industry and is a Global clinical CRO with 25 years of experience in a wide range of therapeutic areas. OPIS provides full-service, 360° clinical trial support from study concept creation and protocol development to full project execution, study data handling and up to study closure, analysis, and reporting.
OPIS
Optimapharm is a globally operating, leading, mid-sized, full-service CRO aiming to deliver new therapies to improve and save patients’ lives.
Optimapharm conducts phase I – IV studies in all therapeutic areas, including complex medical device studies.
With 26 strategically located offices, Optimapharm is giving unrivalled access to patients and investigators worldwide.
Optimapharm
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PHARMExcel is an award-winning, full-service Contract Research Organisation (CRO) providing a flexible and innovative approach to clinical trial delivery. The company is recognised for its in-depth knowledge and experience of the clinical research environment, particularly in the UK, and has a network of regulatory and industry associates, allowing it to provide a global reach.
PHARMExcel
​PHARMASEAL was founded in 2016 by a team of industry leaders who share a vision to create smarter technologies and innovative products for the improvement of human health. The company’s SaaS platform Engility® simplifies the management and control of clinical trials for biopharmaceutical, CRO and medical device companies. Engility® utilises advanced engineering offering enterprise management with rapid deployment, an intuitive user interface and interoperability with other eClinical applications to optimise trial governance and oversight.
Pharmaseal
PCI is a leading global CDMO, providing clients with integrated end-to-end drug development, manufacturing and packaging capabilities that increase their products’ speed to market and opportunities for commercial success. PCI brings the proven experience that comes with more than 90 successful product launches each year and over five decades in the healthcare services business. Leading technology and continued investment enable us to address global drug development needs throughout the entire product life cycle – from manufacturing capabilities through the clinical trial supply chain and into commercialization.
PCI
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Pro-ficiency is a next-generation learning engine for clinical trials. This custom, online, protocol-specific training can help to boost site performance, optimize enrollment, and improve protocol compliance and execution. Pro-ficiency is redefining the learning outcomes learners and leaders should expect from your training investment.
Pro-ficiency
PSI CRO is a privately-owned, full-service clinical research organization (CRO). PSI’s global reach supports clinical trials across the world, specializing in the planning and execution of pivotal registration clinical trials. PSI is committed to being the best CRO in the world as measured by its employees, customers, investigators, and vendors.
PSI CRO
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Pharma Solutions is a specialty pharmaceutical company providing Critical care support to the medical fraternity.
Based in Dubai and operating in 12 Middle Eastern markets, Pharma Solutions specializes in Comparator Sourcing, Clinical Trials Supply, Oncology medications, Haematology, Rare Diseases and Shortage Pharmaceuticals to all Key global authorities, sponsors, and hospitals.
Pharma Solutions
Prevail InfoWorks is a global full service Clinical Research Organization (CRO) and Functional Service Provider (FSP) with a unique combination of clinical operations expertise, the full suite of proprietary clinical trial systems, and advanced analytics. Prevail's uniquely powerful digital tools for clinical analysis are delivered alongside The Single Interface®, a service allowing you to access all your third party and internal data sources with just one role-based login.
Prevail InfoWorks
Premier Research
Premier Research, a clinical research company, is dedicated to helping biotech, specialty pharma, and device innovators transform life-changing ideas and breakthrough science into new medical treatments.
As a global company, Premier Research specializes in the use of innovative technologies for smart study design and trial management to deliver clean, conclusive data to sponsors.
Whether it's developing product lifecycle strategies, reducing clinical development cycle times, securing access to patients, navigating global regulations, maximizing the impact of limited rare disease data, or providing expertise in specific therapeutic areas, Premier Research is committed to helping its customers answer the unmet needs of patients across a broad range of medical conditions.
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Clinical Services International
Clinical Services International (CSI) provides the most comprehensive solutions to clinical trial supplies including sourcing of medicines and devices, distribution and all services needed for successful conduct of studies.
We have offered our solution to more than 1000 clinical trials all over the world.
Headquartered in London and with operations in 5 continents, we provide efficient solutions to the most complex adaptive trials worldwide.
We accelerate drug development and reduce timelines by providing a fully integrated service.
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Address Regulatory, Quality, Operational, Clinical Requirements, and Forecasting
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Manage the entire supply chain and offer tailor-made solutions
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Comprehensive expertise in Oncology and Biosimilar products
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Direct access to all major Pharmaceutical Manufacturers and more than 95 audited suppliers globally.
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Trusted partner of leading Biopharmaceuticals, CROs and CMOs.
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RxSource
Founded in 2005, RxSource in an experienced provider of Clinical Supply packaging and labelling, distribution, and comparator/ancillary sourcing services. We support global clinical trials at all phases through our facilities in the US, EU and Canada in addition to our network of approved depot partners.
Randox Health
Following decades of pioneering research and development, Randox Health offer clinicians and physicians an unrivalled range and combination of tests to facilitate effective disease management, screening, and treatment, with over 1,200 tests in our portfolio, white-labelled health checks, and phlebotomy services.
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Suvoda
Suvoda is a global clinical trial technology company specializing in highly complex, life-sustaining studies in therapeutic areas like oncology, CNS, and rare disease. Suvoda empowers clinical trial professionals to manage the most urgent moments in the most urgent trials through IRT, eConsent, and eCOA solutions delivered on a single platform.
The SGS full service CRO offers a broad range of services to the biotechnology and pharmaceutical industry. We cover preclinical drug development and all clinical phases as well as manufacturing control. This includes CDMO, biosafety, GMP testing, bioanalysis, central lab, dedicated CRO with own phase 1 unit and study sites.
SGS
SDC delivers top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. We are committed to providing experienced teams who will take ownership of your needs and are positively engaged in your projects. With strategic consulting, biometric services (biostatistics, data management) and technology solutions (EDC, IRT/RTSM, eSource, data analytics/warehousing) expertise at our core, our services are scalable to provide seamless, full service clinical trial solutions.
Speak with us today to see why SDC is The Right Fit For You.
SDC
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Salvius Legal is a company specialized in all agreement types that are required to perform a clinical trial, with a special focus on site contract management and GDPR compliance support, but also including review and negotiation of e.g., vendor and ancillary contracts. It has site contracting experience in practically every country where clinical trials are performed, and as such the knowledge of applicable laws and regulations, and different local or regional contracting customs. Its international team of lawyers and contract managers with understanding of the clinical trial process, industry requirements and different stakeholders involved, is fully equipped to assist your organization with managing this part of the clinical trial start-up phase.
Salvius Legal
SuperNOVA Clinical Research: Empowering Biotech Excellence
Unleash the full potential of your clinical operations with SuperNOVA Clinical Research. Our comprehensive services include:
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Centralized Clinical Trial Imaging Core Lab & Radiology Services
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Clinical Operations & Project Management
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Quality Assurance (GxP, ISO, Inspection Readiness)
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CRO and Sponsor Staffing
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Policy, Risk Management, Compliance, and Governance
Partner with us to turn your vision into measurable results. We offer white-glove, agile, value-driven, and cost-effective solutions with full-service CRO and imaging capabilities.
SuperNOVA Clinical Research
Stiris Research is a full-service, Clinical Trial Management company specialized in conducting Phase I through IIIB trials. We are the only CRO that was formed from listening to the stakeholders engaged in clinical trials, identifying their unmet needs, and developing a unique, value-based approach to address those needs.
Stiris Research
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Sharp Clinical
Sharp Clinical provides a complete range of clinical services from the pre-clinical stage through to commercialization. Our project management and operational teams have vast experience in managing local and global
clinical trial supplies for a wide variety of dosage forms and innovative treatment candidates, including orphan drugs and gene therapies.
Seascape Clinical’s tech platform, ClinOps Pro, helps sponsor clinical operations teams eliminate their busy work (manual, repetitive tasks).
Clients have enjoyed these benefits:
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Lower and streamlined workload, resulting in decreased hiring rate
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Standardized clin ops execution across the entire org
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Less reliance on CRO's reporting
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Faster reporting of trial metrics and risks to senior management by the study team
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Alignment of the entire clin ops “stack”: senior management, program management, and the study team
Seascape Clinical
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Science 37’s mission is to accelerate clinical research by enabling universal trial access for patients. Through our solutions; the Metasite™ and Patient Recruitment, we accelerate enrollment by expanding the reach of clinical trials to patients beyond the traditional site and rigorously qualifying patients prior to referring them to a traditional site. Our solutions are powered by a proprietary technology stack with in-house medical and operational experts that enhance quality through standardized workflows and best-in-class study orchestration.
Science 37
Printed packaging solutions for clinical trials
and medication adherence
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Smurfit WestRock partners with our customers to
provide printed packaging solutions for their
Clinical Trial and Adherence focused CR-SF
packaging needs. We offer a complete range of
innovative packaging including multi-vial and
injector cartons, complex calendarised blister
packs, and SMART electronically enabled
platforms. Our business is packaging but our
strength is developing solutions to meet your
requirements. We focus on innovation and
leverage our extensive knowledge of the clinical
trial and drug launch process to create package
solutions that optimise supply chain whilst
improving patient adherence. This is what our
customers have come to expect and value
– and this is what we commit to deliver.
Smurfit Westrock
Thriva Solutions
Thriva Solutions is a UK-based HealthTech company that offers a remote diagnostic testing platform and services to help clinical studies become more diverse, accessible, and secure. We are revolutionising the diagnostics industry by offering innovative testing solutions that are flexible, scalable and convenient. We aim to provide a human-centric experience and focus on diversity, accessibility, and accuracy. By working with Thriva, you can be a part of a robust and impactful scientific future
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TFS HealthScience, a global CRO, collaborates with biotech and pharma firms worldwide in their clinical development. With 800 experts, we offer tailored research services in 40+ countries. Providing full clinical development, strategic resourcing, and solution-driven teams, TFS works for a healthier future, aiming to expedite treatments for patients.
TFS HealthScience
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TCR-Solutions is a boutique, full service, global Clinical Research Organisation established in 2015 to support Biotechnology, Pharmaceutical and Academic sponsors worldwide.
We help these partners navigate the unique and ever-changing hospital environment, through an unrivalled understanding of the people, processes and priorities involved, while always keeping patients at the heart of what we do.
Our sustained ethos of putting hospital sites at the very heart of what we do means we continue to successfully deliver clinical trials across a wide variety of phases and therapeutic areas.
Recent highlights include five important and innovative COVID studies; highly complex first in-man studies; multiple oncology, radiopharmaceutical, gene therapy, psychiatry, and ophthalmology projects; as well as post-marketing Real World Evidence programmes. Over the past 18 months, we have also carved out a niche in medical device studies.
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OPRA, our platform, enhances Risk-Based Quality Management (RBQM) by offering integrated Risk Management, Centralized Monitoring, and Subject Monitoring. It seamlessly automates tasks, improving trial quality, decision-making, and efficiency. Subject Monitoring ensures close oversight of patient data, enhancing safety and compliance, and contributing to team satisfaction. OPRA streamlines trial management, upholding high standards for patient well-being and trial success.
Triumph Research Intelligence
Trialbee is revolutionizing the patient recruitment ecosystem with technology, people, and passion. Featuring the Honey Platform™ to centralize and standardize your funnel, Precision Recruitment for hyper-targeted digital outreach, medical secondary screening for pre-qualified referrals, and our curated Omnichannel Network, Trialbee helps you take control of your global patient recruitment.
Trialbee
Celebrating 21 years of experience, global reach, and clients ranging from diagnostic start-ups to international pharmaceutical companies and CROs. We are at the forefront of a new paradigm in eClinical technology, delivering integrated, flexible, and easily implemented on-demand data management and reporting solutions around the world.
TrialStat’s eClinical Suite consists of a fully unified product offering including EDC, eConsent, Randomization, IWRS & Supply Management, ePRO, Adjudication, Coding, AE/SAE Management, Vendor Neutral Imaging Archive, Validated Nuclear Medicine Viewers, a robust Reporting and Analytics Portal and Custom Validated Development Services. We stand alone in the industry with such an all-compassing suite of capabilities for conducting clinical trials that can also be seamlessly connected to external data sources such as EMR, mobile devices and wearables, imaging, data warehousing, and other Clinical and non-clinical data and information sources.
TrialStat
TRYAL is a leading provider of innovative AI-powered eClinical solutions that leverage cutting-edge technologies to enhance clinical research. With a mission to accelerate study start-up and simplify the complexity of clinical data collection, TRYAL's intelligent platform and eConsent, eCOA, & HomeHealthcare solutions streamline processes, drive study efficiency, and automate system design directly from the protocol.
TRYAL
Trialzen's Forecast & Planning Solution (FPS) is revolutionizing clinical trial supply chain management with its lightning-fast response times and user-friendly interface. Experience empowered decision-making with comprehensive insights and seamless RTSM integration. Our solution offers detailed reporting and a transparent pricing structure, ensuring unparalleled efficiency and maximizing ROI. Join us in accelerating your clinical trials with Trialzen FPS.
Trialzen
TriloDocs is an AI tool that generates an initial draft of a Clinical Study Report that accurately reflects the source material (protocol, statistical analysis plan, data tables and figures). The tool not only creates formatted tables and figures but also meaningful text around them, highlighting clinically relevant findings with no risk of hallucinations or ‘making things up’. The medical writer and the clinical team have a first draft to discuss in a matter of days instead of weeks. The tool is unique – created using over 100 years of medical writing experience.
TriloDocs is created by medical writers for medical writers.
TriloDocs
Thermo Fisher offers comprehensive clinical trial service capabilities including clinical supply optimization, clinical ancillaries, comparator sourcing, global clinical packaging and labeling, storage and clinical logistics, cold chain management, and decentralized trial offerings. With 30 cGMP-compliant sites and over 30+ years of experience advancing clinical trials, we have the resources and global network you need to support clinical trial success.
Thermo Fisher Scientific
TMC is a global clinical research organisation. Its activities are performed by approximately 900 subject-matter industry experts, located in over 70 countries. TMC supports pharma/biotech companies to develop innovative, often life-saving, treatments for rare and oncology diseases, providing tailored solutions and world-class support that responds uniquely to its clients’ requirements.
TMC
Taikun Pharma Services is an expert in global clinical packaging, storage and distribution services. Whether it's optimizing flexibility in clinical supply timelines or assisting with regulatory guidelines and packaging design, Taikun Pharma Services is committed to delivering client centric solutions to support the success of clinical trials globally.
Taikun Pharma Services
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TrialHub is a clinical data intelligence and feasibility platform, powered by Gen AI.
We’re the first platform to combine country, site, and patient feasibility, as well as automate SoC research and connect reimbursed drugs to indications, in over 70 countries.
Instead of fixing clinical trial challenges, we deliver clinical insights, based on real-time and historical data, to help our users prevent and predict them.
TrialHub
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Union Development
Union Development empowers Biotech, Pharma and Medical Device companies, with its worldwide BESTFIT Solutions, DEVOPS Development Ops Management and OMG Outsourcing Management services to leverage global capabilities for Research & Development success.
Our experience in creating stage appropriate, global solutions and connecting passionate solution-providers brings agility, innovation and resource oversight to a new level in the Clinical Research Industry.
Univo IRB, formerly Principal IRB, is a next generation institutional review board (IRB) specializing in the ethical review of Phase I-IV pharmaceutical, device, biologic, behavioral, and psycho-social research. We recently launched OneVerse™ - the industry’s first purpose-built, electronic platform that modernizes the IRB experience. We offer agile study approaches, expert solutions powered by industry-leading study technology, and a service-first approach. Univo IRB holds accreditation through the Association for the Accreditation of Human Research Protection Programs (AAHRPP). With support from senior advisors and 60+ years of industry experience, Univo IRB guides studies to approval while respecting the rights and welfare of patients every step of the way.
Univo IRB
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Voiant
MedQIA, WorldCare Clinical and DARC, have come together to form Voiant, the industry’s leading clinical trial imaging solution provider with unparalleled scientific and clinical domain expertise. Voiant’s unique AI-based software platform integrates all aspects of clinical trial imaging, providing biopharmaceutical companies with high-speed delivery of quality clinical endpoint data.
VCTC
VCTC is the UKs first and only clinical trial site established specifically to address the burden that participants face when taking part in clinical trials. Our virtual and decentralised trials place the participant and the centre of their trial experience, provi