Meet The Team
COG: CRO Summit
Partners
For more information on sponsorship opportunities, please contact Alex O’Leary.
Email: aol@thepbcgroup.com | Phone: +44 (0)7795 345 108.
Premium Partners
​Judi by AG Mednet is the award-winning clinical trial collaboration platform that streamlines workflows and accelerates the process of developing therapies for patients across the world. Trusted by 19 of the top 20 global biopharmaceutical sponsors and 5 of the top 6 global CROs, Judi has delivered over 2500 studies across 170 countries and 71,000 sites to support clinical event and endpoint adjudication, central eligibility review, data safety monitoring boards, medical imaging, and other mission-critical areas of clinical development.
Judi by AG Mednet
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
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
Florence Healthcare is a leading provider of Site Enablement solutions that streamline clinical research operations and improve collaboration among research sites, sponsors, and CROs. With a focus on driving innovation and enhancing the trial site experience through site enablement, Florence Healthcare is committed to closing the cure acceleration gap and revolutionizing the clinical trial industry.
Florence Healthcare
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H1 harnesses and democratizes access to hard-to-assemble HCP information, claims data, ground-breaking research, and expert opinions. H1’s ability to gather and make sense of billions of data points and deliver them in workflow-friendly solutions helps to accelerate the development, launch, and dissemination of life-saving treatments; drive meaningful engagements with key opinion leaders; and help ensure equitable access to healthcare services.
H1
Revolutionize and simplify how your firm manages information with the leading record, document, and information management platform. Automate SOPs and resolve CAPAs efficiently through programmed workflows and alerts. Enhance researcher productivity by streamlining complex documentation tasks. Provide evidence of operational oversight that inspires confidence in sponsors and meets regulatory requirements. All while leveraging M-Files' powerful GenAI. Get connected with a scalable solution.
M-Files
Exhibition Partners
The Biomedical Research Alliance of New York (BRANY) is a national organization providing support services to sponsors, CRO's and investigators involved in research in a wide variety of therapeutic areas, medical devices, biologic and diagnostic trials. Staffed by multi-disciplinary experts, BRANY is an expedited "end-to-end solution"​ for clinical trials. BRANY is able to offer its partners a turnkey solution for expedited site identification and study start-up (SMART-Start-60), Central IRB Services, IBC services, Medicare Coverage Analysis Services, Research Education, and Quality Assurance auditing and consulting services. BRANY was founded in 1998 by nationally-ranked academic medical centers, which today includes: NYU School of Medicine, Montefiore Medical Center, Mount Sinai School of Medicine, and North Shore-Long Island Jewish Health System.
BRANY
Block Clinical is a site and patient services company focused on streamlining payment workflows and global patient travel and concierge services. Our purpose built software platform automates site payments, patient stipends and reimbursements while facilitating global patient travel and capturing transactions in real time via our integrated network of suppliers.
Block Clinical
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
Court Square Group (CSG) delivers secure, compliant, and AI-enabled technology solutions purpose-built for CROs and life-science organizations. Our Audit Ready Compliant Cloud™ (ARCC) provides a fully validated, 21 CFR Part 11/Annex 11–aligned environment ensuring continuous audit readiness and hardened security. Built on ARCC, RegDocs365® uses advanced AI/ML to streamline TMF operations, automate document classification, accelerate submission preparation, and improve regulated content accuracy. Supported by our GxP-focused Managed Services, CSG provides end-to-end cloud, validation, security, and data lifecycle operations—helping CROs reduce operational burden, enhance compliance, and accelerate study delivery with confidence.
Court Square Group
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 Labs
The DPO Centre is the leading provider of outsourced data privacy resources for life sciences organisations. We provide highly experienced and qualified Data Protection Officers (DPO) and Data Protection Representatives (DPR), who possess a deep understanding of the specific requirements of the industry.
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Having supported over 1,000 clients globally, the company serves a broad range of bioscience, genomics, therapeutics, healthcare and pharma companies. With offices in London, Toronto, New York, Dublin and Amsterdam, as well as a network of establishments in all 27 EU Member States, we have the reach and the expertise to meet the diverse privacy needs of life sciences organisations worldwide.
The DPO Centre
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
InfoPathways partners with organizations to build secure, compliant, and efficient IT environments. We provide managed technology services including help desk, cybersecurity, and data management solutions designed for research settings. We’re here to help you safeguard data integrity, meet audit requirements, and keep your team focused on innovation, not IT headaches.
InfoPathways
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
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
At MyCardium AI, we empower cardiac clinical trials through precision, intelligence, and scale. Founded in 2022 as a spin-out from University College London, we combine over 15 years of academic research with world-leading expertise in heart failure, amyloidosis, Fabry’s, and cardiomyopathies. Our dedicated Core Lab specializes in cardiac MRI and echocardiography, using proprietary AI to deliver up to 40% greater measurement precision, accelerating trial timelines and reducing required sample sizes. With regulatory-grade quality (FDA, CE, ISO), scalable infrastructure, and expert oversight, we offer end-to-end support for global trials, from site onboarding to centralised cardiac safety screening.
MyCardium AI
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
​PHARMASEAL was founded in 2016 by a team of industry leaders who share a vision to create smarter technologies and innovative products for the improvement of human health. The company’s SaaS platform Engility® simplifies the management and control of clinical trials for biopharmaceutical, CRO and medical device companies. Engility® utilises advanced engineering offering enterprise management with rapid deployment, an intuitive user interface and interoperability with other eClinical applications to optimise trial governance and oversight.
Pharmaseal
Slope drives operational excellence for highly complex, sample-intensive, early-phase clinical trials. The platform transforms chaotic clinical trial supply chains into protocol-specific operational workflows for sponsors, CROs, labs, and clinical research sites. Through Slope’s clinical inventory, sample management, and data-driven resupply solutions, the platform enables stakeholder collaboration, real-time visibility, traceable chain of custody, and risk mitigation. The results are improved trial outcomes including boosting patient enrollment and retention, reduction of supply waste, adherence to study protocols, and timelines and budgets. Slope has managed over a million supplies for thousands of studies across hundreds of sites.
Slope
Tanner Pharma, a US-based company with over 20 years of experience, supports global clinical trials. Our new US GMP facility offers comparator sourcing, packaging, labelling, kitting, storage, and distribution. With a global network, we ensure efficient and reliable sourcing and tailor our services to meet your needs.
Tanner Pharma
The Braff Group is the leading mergers and acquisitions advisory firm specializing
exclusively in health care services, including Outsourced Pharma Services,
Health Care Staffing, Behavioral Health, Home Health, HME, Home Infusion &
Specialty Rx, and Adjacent Services. Founded in 1998, they have completed more than 385 deals.
The Braff Group
The Patient Recruiting Agency™ (TPRA) is a full-service Global Patient Recruiting & Retention Company working for Sponsors, CROs, & Investigators.
With over 25 years’ experience, TPRA has completed hundreds of campaigns enrolling over 10,000 patients of all ages and races for more than 150 healthy, disease-specific, rare, and hard-to-reach indications in multiple languages in over 45 countries. | Flexible. Scalable. Experienced. |
TRPA
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
Univo IRB
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.
Associate Partners
Advarra is #1 in trusted research review services, innovative site and sponsor technology, and the pioneer in clinical research experience software. Our unique portfolio of technology and services reduces friction by decreasing technology burden, improving study visibility, and enabling smarter decisions that advance clinical research. For more information,
Advarra
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
Medrio
With almost two decades of experience, Medrio delivers proven, scalable solutions and unrivaled customer support to sponsors, CROs, and sites worldwide. The company’s suite of solutions, including CDMS/EDC, eCOA/ePRO, eConsent, and RTSM, enables the capture of quality clinical trial data while optimizing workflows for regulatory readiness. Experience the power of Medrio and realize the full potential of your clinical operations and outcomes
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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.
Suvoda
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Woodley Trial Solutions support clinical trials worldwide with equipment supply and dedicated added value services.
Our experience, product knowledge, sourcing capability and logistical knowhow earmark us as experts in our field.
Whatever equipment you need for your study, we ensure it arrives wherever and whenever you need it.
Worldwide Clinical Trials
Networking Partners
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)
Supporting Partner
NCBiotech is a private, non-profit corporation established by the state of North Carolina to foster growth in the state's life sciences industry. Its mission is to accelerate economic development through innovation, commercialization, education, and business growth. The organization supports companies with funding through grants and loans, provides business development services, and works to develop talent and infrastructure to strengthen North Carolina's position as a global leader in the life sciences.
NC Biotech
