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
Exhibition Partners
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
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
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
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
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
Viedoc
At Viedoc, we design engaging software that modernizes clinical research so that necessary treatments can reach the people who need them faster. We accomplish this by combining technology and a creative design to streamline, automate and simplify conventional processes within clinical research. Viedoc makes every aspect of a clinical study a bit smoother, resulting in greater discoveries that make a difference and has the potential to improve lives.
Associate Partners
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 Partner
