Meet The Team
COG New England
2026 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 more than a leading CRO - we are a strategic partner dedicated to driving your programme forward with confidence. We
deliver hands-on guidance, deep industry expertise, and a responsive, collaborative approach that ensures progress at every stage.
Aixial Group combines extensive therapeutic expertise in oncology, CNS, rare diseases, and radiopharmaceuticals with a global team
of more than 1,000 employees, to deliver adaptable CRO solutions, including full-service support, functional service provision, and consulting.
Everything we do is focused on what truly matters: achieving positive outcomes for our clients and their patients.
Aixial Group
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.
Mednet
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Harbor Clinical is a women-owned clinical research services firm with headquarters in the Boston biotech area. As a Functional Service Provider (FSP) offering Staff Augmentation, Consulting, and Single-Service resourcing models, Harbor Clinical's core competencies include:
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Quality Assurance (Inspection Readiness, site/vendor audits, etc)
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Vendor Oversight
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Clinical Operations
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Data Management
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Programming
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Biostatistics
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Medical and Safety Management
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Medical Writing
Harbor Clinical
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Premier Research
Premier Research, a global clinical research, product development, and consulting company, is dedicated to helping innovators transform life-changing ideas and breakthrough science into new medical treatments. We offer strategic solutions across the entire development lifecycle, from pre-clinical through commercialization, specializing in smart study design and full-service clinical trial management.
Leveraging technology and therapeutic expertise, we deliver clean, conclusive data with a focus on reducing development timelines, securing access to the right patients, and effectively navigating global regulations to ensure submission-ready results.
As an organization that puts patients first, we pride ourselves on helping customers answer the unmet needs of patients across a broad range of medical conditions.
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
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.
SDC
Content Partners
IQVIA Biotech delivers flexible clinical solutions designed to help biotech and emerging biopharma companies get treatments to patients. Our clinical development team brings expertise from two decades of planning and executing clinical trials exclusively for biotech companies. Drawing on IQVIA's unparalleled data and advanced analytics, IQVIA Biotech creates intelligent connections to deliver powerful insights to help customers accelerate clinical development of innovative medical treatments.
IQVIA Biotech
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PhaseV is a clinical development technology company that leverages advanced causal machine learning, generative AI, and real-world data to design and optimize smarter trials. By enabling adaptive, data-driven decision-making, PhaseV helps biopharma teams accelerate development, reduce uncertainty, and run more efficient, patient-centric studies across therapeutic areas.
PhaseV
Exhibition Partners
Alturas Analytics is a GLP compliant bioanalytical CRO specializing in LC-MS/MS solutions supporting preclinical and clinical research, IND submissions, and New Drug Applications.
In addition to providing PK support services to pharmaceutical companies worldwide, Alturas maintains an intensive research effort to apply new technologies toward scientific advancement. Our success is built on developing long-term relationships with clients by delivering high-quality bioanalytical results in a timely manner.
Alturas Analytics
CTI Labs provides specialized laboratory services tailored to the needs of CROs, including bioanalytical testing, biomarker development, and custom assay design. As part of CTI, a global, full-service CRO, CTI Labs brings decades of clinical research experience and a collaborative approach to help CROs deliver high-quality data and accelerate development timelines. With deep expertise in rare disease and advanced therapies, CTI Labs ensures scientific precision, regulatory compliance, and operational efficiency across every stage of clinical development.
CTI
HiRO is a global, boutique CRO based out of Somerset, NJ partnering with biotechs developing life changing treatments to save lives. Our flexible, fit-for-purpose model leverages our expertise to accelerate your clinical development.
HiRO
MLM Medical Labs is an international central and specialty laboratory with harmonized operations in Europe, North America, and South Africa. With over 30 years of experience, MLM supports more than 400 clinical trials at any given time, offering services including central lab testing, biomarker discovery, kit building, assay development, and long-term sample storage. MLM is known for scientific expertise, rapid startup, flexible logistics, and full regulatory compliance.
MLM Medical Labs
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
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
Ephicacy is a fast-growing biometrics CRO headquartered in Iselin, NJ, with operations across North America, India, and Europe. Our experienced team provides scalable statistical programming, biostatistics, data management, real-world data analytics, and clinical literature review services to pharmaceutical and biotech companies. Founded in 2005, we help clients accelerate time to market cost-effectively.
Ephicacy
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
Ovid, by Wolters Kluwer
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.
SGS
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?
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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.
Clin.AI
Total Trials, formerly known as FHI Clinical is a full-service contract research organization (CRO) with the global expertise, responsive approaches and proven solutions to manage complex clinical research around the world. Benefitting from our 50+ year history of clinical research, our team of over 200 global staff have worked on studies in nearly 75 countries. As problem solvers, forward thinkers and on-the-ground members of those communities, we’re dedicated to helping you find solutions to the research challenges that have kept life-saving medicines from at-risk populations.
Total Trials
METRONOMIA is your Data Science CRO for biostatistical services and consulting, clinical data management, and medical writing.
Since 1990, we have supported over 720 projects in all clinical development phases and major therapeutic areas.
Our team of 140+ highly skilled employees serves the needs of our pharma-, biotech-, and medical device customers with the highest degree of flexibility, reliability and quality.
METRONOMIA
Phastar is an award-winning biometrics and data science CRO, trusted by pharma, biotech, and medical device companies worldwide. Our global team delivers precise, high-quality data using AI-enhanced analytics, advanced statistics, and deep therapeutic expertise. We simplify complexity, accelerate trials, ensure compliance, and bring life-changing therapies to patients faster.
Pharstar
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
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.
Associate Partners
Almac
Almac Clinical Services have been partnering with clients for 30+ years, we set the standard for developing effective supply chain strategies that ensures our sponsors can overcome their unique challenges and deliver supply continuity to patients wherever they are in the world.
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We have a range of tools and services to help you achieve this, from forecasting/inventory management, supply chain strategy to global logistics management, end-to-end temperature solutions, IRT set-up and strategy, direct to patient distribution and pharmacy services alongside our clinical packaging and labelling facilities.
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When you partner with Almac you are partnering with experts who Supply With Care.
Optimapharm
Optimapharm is a globally operating, leading, mid-sized, full-service CRO aiming to deliver new therapies to improve and save patients’ lives.
Whether a pharmaceutical, biotech, or medical device company, we are your ideal mid-sized, full-service CRO.
Our in-depth expertise and long-lasting experience, combined with a flexible and collaborative approach, allow us to tailor our responses to each individual study.
Our clinical development capabilities span trial Phases I-IV, across a broad range of therapeutic areas, including medical devices.
We have an excellent track record for supporting a range of stakeholders in the pharmaceutical industry, including sponsors and research institutions at each clinical development phase.
ProofPilot modernizes the way clinical trials are launched and managed. With a focus on simplifying site operations and reducing patient burden, the platform deploys a seamless, branded experience from startup through closeout, leading to faster enrollment timelines, higher compliance rates and increased quality for your trials.
Trialmed
Trialmed is the trusted clinical trial partner for patients and sponsors/CROs. We facilitate clinical research as a care option for patients and healthy volunteers as a part of their health care journey. We create holistic experiences that put the patient first through our welcoming clinics and focus on quality delivery.
Networking Partners
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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)
