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.
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
Premium Partners
Endpoint Clinical is an interactive response technology (IRT) solutions provider that supports the life sciences industry. Our innovative, high-quality randomization and clinical trial management technologies are backed by over a decade of award-winning experience and expertise. Endpoint is headquartered in Wakefield, MA, with offices across the US, EU, and Asia.
Endpoint
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
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
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
TRYAL is a leading provider of innovative AI-powered eClinical solutions that leverage cutting-edge technologies to enhance clinical research. With a mission to accelerate study start-up and simplify the complexity of clinical data collection, TRYAL's intelligent platform and eConsent, eCOA, & HomeHealthcare solutions streamline processes, drive study efficiency, and automate system design directly from the protocol.
TRYAL
Exhibition Partners
BioBridges
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.
Block Clinical
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.
BRANY
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.
Clario is a leading healthcare research and technology company that generates high quality clinical evidence for our pharmaceutical, biotech, and medical device partners. We offer comprehensive evidence generation solutions that combine eCOA, cardiac solutions, medical imaging, precision motion, and respiratory endpoints.
Clario
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
MyData-TRUST is a complete solution provider for Data Protection/Privacy dedicated to Life Sciences and support throughout the product lifecycle. We offer full-board services to companies collecting health/clinical data such as Biotechs, Pharmas, Medtechs, Hospitals, eHealth and CROs.
Global Data Protection/Privacy regulations coverage includes: UK GDPR, US regulations (HIPAA, California-CCPA/CPRA), Australia APP, Canada PIPEDA, EU GDPR, Swiss FADP, US-HIPAA, California CCPA/CPRA, and Brazilian LGPD.
Core teams are equipped to address any Legal, Clinical Operation or Cyber Security concerns related to global Data Protect on Regulations.
Clinical Data Protection Officers can provide direct operational support, including risk
assessments, procedure development, and compliance tools tailored to your requirements. This distinctive blend of expertise ensures comprehensive coverage of all aspects of Data Protection and Privacy.
MyData-TRUST
Trusted science-led solutions
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Time after time, the global bio-pharmaceutical industry turns to us for the high-quality data they need to bring essential treatments to patients faster. We are the industry’s most trusted provider of preclinical to late-phase imaging solutions and Randomization and Trial Supply Management (RTSM).
Perceptive eclinical
Prevail InfoWorks is a global full service Clinical Research Organization (CRO) and Functional Service Provider (FSP) with a unique combination of clinical operations expertise, the full suite of proprietary clinical trial systems, and advanced analytics. Prevail's uniquely powerful digital tools for clinical analysis are delivered alongside The Single Interface®, a service allowing you to access all your third party and internal data sources with just one role-based login.
Prevail InfoWorks
Sabai IRB Services provides quality-driven, personalized ethical reviews for multi-therapeutic research through its AAHRPP-accredited IRBs. The Sabai IBC team provides expert IBC Reviews for oncology, rare disease, and gene transfer/therapy clinical trials as a central IBC and through Concierge support to local IBCs. We lead with science and differentiate with service. Experience what Sabai can do for you, and what we can do together to advance development and access to treatments.
Sabai
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
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. | PatientRecruiting.com
The Patient Recruiting Agency™ (TPRA)
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, 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
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
CTI Laboratories offer an array of comprehensive services tailored to meet your requirements. As a global provider of full-service laboratory operations, we offer comprehensive lab services that include safety testing, biorepository, kitting, PBMC processing, bioanalytics, PK/PD testing, and drug modeling. We provide a consultative approach to laboratory requirements and study set-up, along with the capability and expertise to oversee these procedures effectively.
CTI Laboratories
​HeartcoR Solutions (HCS) is a leading Cardiac Safety Core Lab serving the Medical Device and Pharmaceutical Industries. HeartcoR has conducted 32 global IDE-PMA study projects since 2018 and has extensive understanding of Cardiac Safety execution to yield high study subject compliance in support of regulatory submissions. HCS’ also serves Bio-Pharmaceutical companies conducting intensive QT and phase I-IV safety studies. The Company’s 50 employees hold a required certifications and our Electrophysiologist/Cardiologist analysis team are recognized experts in heart rhythm analysis. HeartcoR is based in Schaumburg Illinois, twenty minutes north of O’Hare Airport.
HeartcoR Solutions
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
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
Medrio
Science 37’s mission is to accelerate clinical research by enabling universal trial access for patients. Through our solutions; the Metasite™ and Patient Recruitment, we accelerate enrollment by expanding the reach of clinical trials to patients beyond the traditional site and rigorously qualifying patients prior to referring them to a traditional site. Our solutions are powered by a proprietary technology stack with in-house medical and operational experts that enhance quality through standardized workflows and best-in-class study orchestration.
Science 37
Suvoda
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.
uMotif
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.
Woodley Trial Solutions
Yonalink
Yonalink is a full data collection and management solution for sponsors, CROs, and site.
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Our solution automates data collection from patients, medical devices, and EHRs, replacing today's manual data collection processes, improving trial efficiency, and reducing staff burnout.