Meet The Team
COG New England
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
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
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
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.
Myonex
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
Versiti Clinical Trials
Versiti Clinical Trials brings together the best of multiple specialty organizations offering central lab, complex diagnostics, quality and regulatory strategy, and CRO services to act as an extension of your organization’s internal capabilities. With deep therapeutic expertise, consultative practices, and scalable solutions, we deliver a right-sized approach tailored to your unique research and development needs.
Content Partners
A2 Healthcare (A2) is a Japan-Taiwan industry leading clinical CRO with more than 1,300 employees. A2 have opened its new US office in Boston area in 2023. A2 is the expert for clinical development in Japan and Taiwan and are interested to support US pharma/biotech to reach out to its region. Also have a unique program to invest in their pipeline, especially for drugs which are already marketed or under development in US.
A2 Healthcare
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
Recruitment Partner
RBW Consulting
RBW Consulting is a life sciences recruitment and search consultancy with purpose operating in the US, UK and Europe. By giving clients the people, insight and networks to innovate and scale, its teams are able to help life sciences businesses change the world.
RBW Consulting also gives back by playing an active role in directly funding initiatives that support better health and wellbeing.
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
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
Egnyte for Life Sciences delivers a secure, intelligent content and data management platform for biotechs. Our platform facilitates secure and compliant collaboration throughout all R&D stages, adapting to your unique needs with flexible solutions for eTMF, SCE, and Controlled Documents. Seamlessly integrating with your existing systems, Egnyte helps accelerate your path to market by streamlining processes and ensuring secure access to critical information.
Egnyte
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
Leapcure connects patients with clinical trials to make research more equitable and efficient with patient advocacy at the forefront. Patients are the experts in their condition and advocacy groups provide a platform for patient voices, and Leapcure is expert at discovering them efficiently. Working directly with these communities is the key to pushing research forward in an inclusive way. EQuitable clinical trials are trials where empathy and emotional intelligence are crucial, helping to build trusted connections between sponsors, sites, KOLs, and patients.
Leapcure
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
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
Univo IRB, formerly Principal IRB, is a next generation institutional review board (IRB) specializing in the ethical review of Phase I-IV pharmaceutical, device, biologic, behavioral, and psycho-social research. We recently launched OneVerse™ - the industry’s first purpose-built, electronic platform that modernizes the IRB experience. We offer agile study approaches, expert solutions powered by industry-leading study technology, and a service-first approach. Univo IRB holds accreditation through the Association for the Accreditation of Human Research Protection Programs (AAHRPP). With support from senior advisors and 60+ years of industry experience, Univo IRB guides studies to approval while respecting the rights and welfare of patients every step of the way.
Univo IRB
Associate Partners
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.
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.