Meet The Team
COG Europe
Partners
For more information on sponsorship opportunities, please contact Alex O’Leary.
Email: aol@thepbcgroup.com | Phone: +44 (0)7795 345 108.
Premium 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.
Aixial Group
CMIC Group is Japan’s largest clinical CRO with global reach. We offer drug development, GMP manufacturing, clinical site management, regulatory consulting, and contract sales support. CMIC helps pharmaceutical, biotech, and medical device companies enter Japan, run trials across Asia, and bridge drug development and manufacturing between the US and Japan.
CMIC
Evestia Clinical is a global CRO built for biotech. We specialize in oncology, rare disease and neurology, areas where complexity and urgency meet real patient need. With offices across Europe, North America, and APAC, we support trials from early-phase to pivotal, offering full-service delivery, FSP models, and platform solutions. Our teams integrate seamlessly, move quickly, and stay close to the science. Sponsors trust us for our continuity, strategic thinking, and biotech-first mindset. We’re especially focused on inclusive, patient-centric approaches because representation matters. If you're navigating challenging studies or scaling fast, we’d love to connect with you at the show.
Evestia Clinical
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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
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
Viedoc
At Viedoc, we design engaging software that modernizes clinical research so that necessary treatments can reach the people who need them faster. We accomplish this by combining technology and a creative design to streamline, automate and simplify conventional processes within clinical research. Viedoc makes every aspect of a clinical study a bit smoother, resulting in greater discoveries that make a difference and has the potential to improve lives.
Content Partner
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
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.
Salvius Legal
Recruitment Partner
Founded in 2017, Verbatim Pharma is an independently owned recruitment company specialising in placing mid to senior professionals specifically into the Clinical Trials space. With 15 consultants dedicated to solely this niche, we operate in the US, Europe and the UK, partnering with a broad range of organisations, all of whom contribute to clinical trials.
Verbatim Pharma
Exhibition Partners
Centre for Human Drug Research (CHDR) is an independent clinical research institute based in Leiden, The Netherlands. Founded in 1987, CHDR specialises in early-phase drug development, conducting proof-of-pharmacology and proof-of-concept studies across diverse therapeutic areas.
Centre for Human Drug Research (CHDR)
​Enovalife (formerly Business & Decision Life Sciences) is a global provider of expert CRO and data services to biotech and pharma companies of all sizes. With over 15 years of experience in biometrics, CDISC standards, medical communication, and publications management, we offer top-tier consultants for your workload needs and deliver expert outsourced services on fixed-price, time-bound schedules. Discover how our Belgium-based service centers can support your future projects during COG25 in Amsterdam.
Enovalife
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
Coronado Research is a consultancy-led, professional services organisation, which provides support to pharmaceutical, biotechnology, and medical device companies. Our objective is to optimise the clinical development process by leveraging all the data available using AI, ML, and leading technologies.
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Our practices cover Digital Innovation, Clinical Development, Regulatory, Market Access and HEOR (Health Economics and Outcomes Research), and Medical Affairs. Our teams work with customers to “join-the-dots” between these disciplines to ensure treatments are developed with the end in mind and better match market needs
Coronado Research
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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
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
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
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 Pharmaceuticals
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​LINK Medical is a Nordic full-service CRO and regulatory consulting company providing services for drug development and medical device clients. With expertise across all trial phases, regulatory affairs, and market access, LINK Medical delivers efficient, high-quality solutions to accelerate innovation and improve patient outcomes globally.
Link Medical
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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
Novotech is a globally recognized full-service clinical research organization (CRO) and scientific advisory partner for biotech and small- to mid-sized pharmaceutical companies seeking to advance drug development. With deep therapeutic and regulatory expertise and an expansive global footprint across the Asia-Pacific region, North America, and Europe, Novotech offers clients an accelerated path to bring life-changing therapies to market.
Novotech
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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
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.
MLM Medical Labs
Nucleus Network is the world leader in designing and delivering First-in-Human (FIH) and Phase I clinical trials, with an unmatched track record of over 2,500 Phase I studies conducted across 30+ years. With four experienced clinical pharmacology units strategically located across three key global regions, we offer unparalleled reach, scalability, and speed to market.
Hammersmith Medicines Research, a Nucleus Network Company
Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we save precious time and money in getting drugs to patients. Everything we do for our customers is driven by an unswerving belief that ideas need to become solutions, molecules need to become cures, fast. Because humanity needs solutions, fast.
Quotient Sciences
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.
Scout proudly celebrates 30 years of empowering clinical trials with people-first solutions through Scout Meetings, Scout Clinical, and Scout Academy. Operating in 100+ countries, we deliver face-to-face, virtual, and hybrid clinical meeting planning, patient payment, travel and logistics support, and virtual collaboration and education for top pharmaceutical and biotechnology companies.
Scout
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.
Suvoda
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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
Vantage BioTrials
At Vantage BioTrials, our mission is to advance the clinical development and research landscape by leveraging innovative, risk-based clinical trial management strategies tailored to the life sciences sector. We prioritize patient safety while accelerating the development and market introduction of groundbreaking therapies, ensuring efficient, reliable trials that mitigate risk, drive medical progress, and improve patient outcomes.
Xerimis is a privately held clinical packaging and distribution firm specializing in the needs of clinical trial sponsors for phase I trials through phase IV global trials. Xerimis has focused on clinical packaging and distribution throughout 23 years in existence. Xerimis has 3 wholly owned and managed depots; Philadelphia (US), Reading, (UK) and a new depot in Amsterdam (opened 2024). In addition, Xerimis has an established a network of audited and qualified depots strategically placed throughout the world. Xerimis focuses on supporting small to mid-sized sponsor companies.
Xerimis
Associate Partners
At admedicum, we elevate clinical trial processes by co-creating with patients tailored solutions, providing empathetic recruitment support, guiding participants throughout their journey, and improving communication. Our modular services capture patient experience data through trial participant interviews, enhance trial designs, and support market
admedicum
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
CRS and Venn Life Sciences, part of the hVIVO Group, offer early-phase drug development services. CRS specialises in clinical trials including first-in-human and specialist populations. Venn provides consulting and biometry services across drug development stages, covering regulatory, CMC, PK, and biostatistics, supporting projects from preclinical to marketing authorisation.
eClinical Solutions’ industry-leading data & analytics platform, elluminate®, and biometrics services experts help biopharma researchers at large, mid-size, and emerging life sciences organizations manage trial complexity in less time and with fewer resources. Clients get accurate and timely data insights for better decision-making – enabling them to reduce cycle times, improve productivity, easily scale, and develop tomorrow’s breakthroughs with today’s resources.
eClinical Solutions
NoyMed is a specialized biometrics CRO established in 2017. As a client-focused company, we prioritize the success and satisfaction of our clients. We are committed to building long-term relationships by consistently exceeding expectations and ensuring satisfaction at every stage of our collaboration.
With comprehensive capabilities across Data Management and Statistics, NoyMed supports Phase I-IV studies for pharmaceutical, biotechnology, medical device companies, and research institutes worldwide. Our extensive experience covers clinical trials across various therapeutic areas, including oncology, allergy and respiratory, cardiovascular, neurology/central nervous system, anti-infectives, ophthalmology, dermatology, gastroenterology, vaccines, diabetes/metabolic diseases, and more.
We enhance our operations through advanced technologies that automate and streamline processes, and maintain a global presence with a centrally managed structure.''
NoyMed
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Rho
Rho, a global CRO headquartered in North Carolina’s Research Triangle Park, delivers comprehensive drug development services, from strategy to clinical trials and marketing applications. With more than 40 years’ experience, Rho partners with leading pharmaceutical, biotech, and government organizations, fostering collaboration to accelerate timelines, optimize ROI, and enhance program efficiency.
Unilabs
Networking Partners
Media Partner
International Clinical Trials (ICT) is a specialist journal that discusses the various stages of clinical trials programmes, the funding behind them, and the trends that dictate their feasibility.
Published quarterly, the journal offers a platform of communication and information-sharing for executive and strategic decision makers, seeking out new trends and marketing opportunities, as well as putting a spotlight on the latest innovations coming to market. ICT is specifically designed to be of interest to those actively seeking to source services for improved efficiency in what is an increasingly competitive market.
Prompted by the synergies between trial operations and wider contract research and outsourcing issues, ICT joined forces with sister title European Pharmaceutical Contractor (EPC) in late-2015, in a move that brings added value to both brands. With EPC now an inserted edition within ICT, industry practitioners across these complementary subject areas now have unrivalled access to a wealth of shared views and analyses.
International Clinical Trials (ICT)
