Meet The Team
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Email: email@example.com | Phone: +44 (0)7795 345 108.
EarlyHealth Group a global pharmaceutical company engaged in rendering healthcare accessible through product development and distribution. With global operating centers in Europe, USA, Middle East and Latin America, our three service pillars: (i) clinical trial sourcing, (ii) global depot service; and (iii) managed access services including patient access, product registration and pharmacovigilance.
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.
Address Regulatory, Quality, Operational, Clinical Requirements, and Forecasting
Manage the entire supply chain and offer tailor-made solutions
Comprehensive expertise in Oncology and Biosimilar products
Direct access to all major Pharmaceutical Manufacturers and more than 95 audited suppliers globally.
Trusted partner of leading Biopharmaceuticals, CROs and CMOs.
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.
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.
At Trilogy, medical writing is our passion. As specialists in regulatory documentation, we provide a service that is more than just writing. Our writers are integral parts of our clients’ teams. We proactively plan, coordinate and write regulatory documents to meet timelines, with a readability that reduces the time for review and approval. For more than 20 years, we have been helping pharmaceutical and biotech companies of all sizes, worldwide, to streamline their documentation processes and make sure their documents communicate clearly and effectively.
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:
Clinical supply management
Integrated formulation development, clinical manufacturing & blinding
Specialty handling (potent, cytotoxic, controlled)
Direct comparator/reference product sourcing
Extensive clinical storage, cold chain capabilities & global distribution
Clinical returns, reconciliation & destruction
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.
Expert Contract Management and Legal Services Partner
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.
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.
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.
ChilliPharm provides Clinical Trial Video Services specifically focused on managing the filming, sharing, storage, facial and audio de-identification of filmed clinical assessments carried out during Phase I-IV Clinical trials for pharmaceutical, biotechnology and academic research sectors
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.
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.
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.
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.
Nubilaria is a Solution Provider with an in-depth and long expertise in Data Management.
Early experiences arise in the Banking Reference Data market in the early 2000s.
Since 2008 Nubilaria provides ICT Services in SaaS for the Clinical Research market.
We developed our proprietary Data Management platform - ACTide® - which embraces a broad ecosystem of modules including eCRF, ePRO/eCOA, eTMF, data cleansing, data recovery, RTSM, security tools, clinical data management and biostatistics.
Our platform has been validated according to industry regulations: FDA 21 CFR part 11, GDPR, GAMP5, ISO 9001 and ISO 27001.
Oximio is a leading supplier of end-to-end clinical trial services bringing experience and expertise to the global clinical research industry. The company has grown organically since inception. It employs over 300 highly skilled, multi-national, employees providing innovative, tailor-made solutions across: Project management, Customs clearance & IOR, Depot & distribution, Return, accountability & destruction, Biosamples management, Labelling , Comparator Sourcing’ Ancillary and Equipment Purchase, Equipment Rental, Direct-to-Patient, Patient Transportation, Home Healthcare Services. With UK headquarters, the company also benefits from depots and customs bonded warehouses in Europe, Middle East and Africa & comprehensive partner depot network further expands the company’s reach to effectively meet the demands of global, clinical trial requirements.
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.
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.
We offer world-class clinical research that helps life science companies to successfully develop the predictive and precision medicines of the future.
We combine the deep expertise and agility of the specialist laboratory with the capacity, breadth and global reach of a central lab. Our unique approach to patient data offers our customers the opportunity to have one partner for all their test services, with regular access and consistent support across all clinical trial phases.
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.
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.
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.
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.
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.
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.
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.
With almost two decades of experience, Medrio delivers proven, scalable solutions and unrivaled customer support to sponsors, CROs, and sites worldwide. The company’s suite of solutions, including CDMS/EDC, eCOA/ePRO, eConsent, and RTSM, enables the capture of quality clinical trial data while optimizing workflows for regulatory readiness. Experience the power of Medrio and realize the full potential of your clinical operations and outcomes
PharmaSols-CRO is a team of experts, delivering excellence in clinical trials in Australia & New Zealand for >20 years. We provide full-service, end-to-end clinical trial solutions to global biotech & pharma. PharmaSols-CRO works collaboratively with sponsors and local networks to provide rapid study start-up, fast recruitment, high-quality data, and cost-effectiveness.
Phatebo GmbH located in the southern part of Germany is one of the fastest growing suppliers for clinical trials.
With our international reach we support clients around the world and provide efficient solutions.
We source quality-assured comparators and reference listed drugs and ensure streamlined operations.
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.