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Partners
For more information on sponsorship opportunities, please contact Alex O’Leary.
Email: aol@thepbcgroup.com | Phone: +44 (0)7795 345 108.
Premium Partners
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.
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.
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.
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.
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TriloDocs is created by medical writers for medical writers.
Content Partners
An efficient and effective clinical supply chain strategy can provide a huge added-value to a pharma/biotechcompany running a drug development program. With a proper demand and supply strategy, an optimized clinical supply chain will shorten the production timelines, significantly reduce the risk of patient drop-off, improve clinical trial timing, and cut the budget.
At Boostcode, we have more than 20 years of expertise in all aspects of the supply chain across multiple industries, with a focus on pharma and biotech. In recent years, we focused our activities on the support to biotech companies wishing to transform their clinical supply chain.
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.
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.
SanaClis is a Global full-service CRO and one of the very few service providers with an extensive array of in-house clinical supply chain, logistics and sourcing skills, offering a comprehensive range of end-to-end solutions for clinical trials worldwide throughout the entire life cycle of the study.
Slope drives operational excellence for highly complex, sample-intensive, early-phase clinical trials. The platform transforms chaotic clinical trial supply chains into protocol-specific operational workflows for sponsors, CROs, labs, and clinical research sites. Through Slope’s clinical inventory, sample management, and data-driven resupply solutions, the platform enables stakeholder collaboration, real-time visibility, traceable chain of custody, and risk mitigation. The results are improved trial outcomes including boosting patient enrollment and retention, reduction of supply waste, adherence to study protocols, and timelines and budgets. Slope has managed over a million supplies for thousands of studies across hundreds of sites.
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.
Exhibition Partners
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.
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.
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.
Clinigen combines market-leading clinical trial supplies such as packaging & labelling, storage and distribution, comparator sourcing, as well as biological sample management services. Part of Clinigen’s global supply chain facility and depot network, we deliver tailored solutions for trials in all stages and offer industry best cycle times.
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.
Curavit - “the world’s first all-virtual CRO” - is positively disrupting clinical research by utilizing digital health technology to design and execute decentralized clinical trials. Curavit moves clinical trials to the cloud, where it brings together world-class researchers, diverse patient populations, and innovative sponsors on its proprietary DCT platform. A start-up with customers, revenue, and two years of operational excellence, Curavit plans to rapidly expand its sales, marketing and solution teams while continuing to evolve its proprietary platform.
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.
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.
​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.
SVMPharma presents DISTILL, 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.
Celebrating 20 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.
Associate Partners
​Avance Clinical is a premium full-service global contract research organization (CRO) providing high-quality clinical research services to the international drug development industry and bringing innovative new drugs to market. For more than two decades, Avance has been recognized for its fast, agile, and adaptive solution-oriented services for biotechnology companies.
Caidya is a multi-therapeutic clinical research organization (CRO) serving innovators worldwide. Focused on delivery excellence and an elevated customer experience, Caidya offers a wide range of clinical services and vast therapeutic expertise, supporting its partners from pre-IND strategy, through clinical development to submission and post-marketing surveillance. Caidya leverages industry-leading and proprietary clinical technology to ensure trial transparency and data-driven decision-making.
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.
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.
​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.
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
The PHOENIX group is active in the pharmaceutical wholesale and pre-wholesale business areas with 224 sites in 29 countries supplying pharmacies, doctors, and medical institutions with medicines and health products. Numerous other products and services for pharmacy customers complete the portfolio – from assistance in advising patients to modern goods management systems to pharmacy cooperation programmes. Around 17,000 pharmacies in 18 countries are members of one of the PHOENIX group’s partnership and cooperation programmes.The company offers Healthcare Logistics and other services to the pharmaceutical industry along the entire supply chain. The PHOENIX group also operates over 3,200 of its own pharmacies in 17 European countries, in which around 185 million patients per year receive expert advice from pharmacists in addition to their medicines.
Precision medicine is in our blood, our cells, our genes, and our name. Precision for Medicine, the full-service global CRO, is purpose-built to accelerate clinical research and development processes to bring life-changing therapeutics to those who need them most. We integrate clinical operations excellence, laboratory expertise, and advanced data sciences to deliver on the promise of personalized therapy; translating research into real-world results and forever reimaging how to get there.
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.
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.
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.
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.
Media Partners
