Meet The Team
COG UK
2025 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
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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.
TCRS
Content Partners
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
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.
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, providing them with more control over how, when, and where they choose to participate.
Expert Contract Management and Legal Service 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
Exhibition Partners
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
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 6 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
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
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
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
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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