Meet The Team
COG Bay Area
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
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
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
Cytel is a global leader in cutting-edge analytical solutions, quantitative methods, and innovative statistical software for the life sciences industry. For nearly four decades, Cytel has pioneered adaptive trial design, using data-driven insights to inform strategy across all phases of drug development and commercialization. Cytel continues to drive innovation in clinical research by accelerating drug development, improving success rates, and delivering better patient outcomes. Headquartered in Cambridge, Massachusetts, Cytel has more than 2,000 employees worldwide.
Cytel
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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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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
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
Content Partner
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Veristat
Veristat is a scientific-minded global clinical research organization (CRO) and consultancy that integrates full service clinical trial execution, regulatory consulting, and strategic planning to rapidly advance the development, approval, and commercialization of your revolutionary therapies around the globe. We specialize in supporting biopharma companies developing the most complex, novel, and rare therapies.
Exhibition Partners
​BioBridges delivers flexible solutions for life sciences companies from discovery through commercialization. Our global reach of expertise, services, and technologies empowers our clients to bring innovative solutions to the patients who need them.
BioBridges
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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
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.
Clin.AI
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.
CRIO
EMB Statistical Solutions, LLC is a niche contract research organization serving the pharmaceutical and biotechnology industries. EMB specializes in Data Management, SAS programming and Statistical Analysis/Reporting. Formed in 2000, EMB has had near perfect retention, is associate owned, and has a proven track record of success. EMB uses a team approach that functions as a seamless partner on projects. Each team member is an expert in their field with an average 20+ years of experience. EMB is Powered by Experience.
EMB Statistical Solutions
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.
FHI Clinical
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
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
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
OWL Oncology Research®, a Functional Service Provider (FSP), is a global network of hundreds of experienced clinical research experts specializing in oncology and rare disease trials. Our commitment is to ensure that your clinical trials are conducted effectively and efficiently so that new and promising treatments become available to the millions of people battling these diseases.
OWL Oncology Research®
PBLs core business is Clinical Trial Services, these services include IP labeling, kitting, storage & distribution. PBL offers storage and distribution for clinical trial materials. PBL is cGMP compliant, FDA registered, CA FDB licensed and QP Audited.
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Our speed, agility offer a benefit to sponsors that our competitors simply do not have.
Pacific BioPharma Logistics
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.
PSI CRO
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.
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
UR Central Labs
At UR Central Labs, we combine the strength of a full-service central laboratory with the agility of an entrepreneurial enterprise—embedded within the University of Rochester Medical Center. Our team specializes in fast, flexible, and consultative lab solutions designed to meet the demands of today’s most complex clinical trial protocols. Backed by decades of experience, we deliver unmatched responsiveness, scientific rigor, and personalized service—every step of the way.
Yourway is the only truly integrated provider of clinical value-chain solutions. From clinical packaging and courier services to storage and distribution, we simplify trial logistics globally. With over 25 years of experience and a personalized approach, we help biopharma clients accelerate timelines and gain full visibility across the clinical supply chain.
Yourway
Associate Partners
At Biorce, we empower pharma, biotech, and CROs to run faster, smarter, and more cost-effective clinical trials with our AI Clinical Trial Assistant. By transforming regulatory data and medical literature into actionable insights, we reduce risk, accelerate study startup, and help bring treatments to patients sooner.
Biorce
​OPIS was founded in 1998 by medical doctors from the Pharma Industry and is a Global clinical CRO with 25 years of experience in a wide range of therapeutic areas. OPIS provides full-service, 360° clinical trial support from study concept creation and protocol development to full project execution, study data handling and up to study closure, analysis, and reporting.
OPIS
DRK Pharma Solutions, based in Switzerland, is a full-service CRO powering global Phase I–IV clinical trials. With 100+ experts and a decade of proven success, we accelerate drug development with precision, compliance, and speed. Our patient-first approach and worldwide network expand access to life-changing therapies across diverse populations.
DRK Pharma Solutions
The PPD™ clinical research business of Thermo Fisher Scientific offers laboratory services for pharmaceutical development. With extensive capabilities and scientific expertise, we deliver outstanding project management and high-quality data that meet regulatory requirements. Our global laboratory network combines a dynamic, innovative approach with award-winning technologies to accelerate drug development success.
Thermo Fisher Scientific
HeartcoR Solutions is a leading ECG Core Laboratory providing expert cardiac safety monitoring services for clinical trial sponsors in the pharmaceutical, medical device and CRO industries. Focused on flexibility, innovation, and quality, we support both site-based and decentralized clinical studies with ECG recording, certified technician analysis, electrophysiologist overreads, and validated data delivery to support our customers’ global regulatory filings.
HeartcoR Solutions
V2 Clinical
V2 Clinical has a proven track record of success with our alternative, stand alone FSP model. What sets us apart is our support from early, preclinical work as well as the continued support in our client’s clinical trial. With over two decades of real-world experience to draw upon, the FSP model has demonstrated an unmatched level of speed and responsiveness, while consistently producing high quality outcomes for our Sponsor partners.
Networking Partners
