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Meet The Team

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COG Europe

For more information on sponsorship opportunities, please contact Alex O’Leary. 

Email: | 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


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.



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.


Content Partners


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.

  • 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.


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.


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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.



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


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.



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

Exhibition Partners

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.


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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


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


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.


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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.


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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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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.

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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.


SuperNOVA Clinical Research: Empowering Biotech Excellence


Unleash the full potential of your clinical operations with SuperNOVA Clinical Research. Our comprehensive services include:


  • Centralized Clinical Trial Imaging Core Lab & Radiology Services

  • Clinical Operations & Project Management

  • Quality Assurance (GxP, ISO, Inspection Readiness)

  • CRO and Sponsor Staffing

  • 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

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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.

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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

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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.


Associate Partners

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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.


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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


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


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.


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