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
Everest Clinical Research
​Everest Clinical Research is a full-service, global CRO managing trials end-to-end—from study feasibility and project management to database lock and final study reports. Everest has deep clinical experience in more than 30 therapeutic areas with extensive expertise in oncology, CNS, infectious and rare diseases. The company insists on operational excellence, providing clients with personalized, flexible and detail-oriented attention—illustrated through its high referral rate. Nearly 98% of its clients are recommended from other satisfied customers.
Since its inception as a biostats and statistical programming center of excellence, Everest has grown every year—recently celebrating its 20th anniversary. Today the company serves more than 100 active clients worldwide from its offices in North America, Europe and Asia.
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
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
Delve Heath
Delve Health is a Virtual Research Organization (VRO) founded in 2017 which now has a global presence, we make clinical research faster, easier and more cost effective for our clients, powering clinical trials with a mix of solutions, including IRT/RTSM, electronic consent, patient engagement applications and remotely collect diaries and patient outcomes directly from a patient's connectable device all from the patient's home, school or workplace.
G&L Healthcare Advisors is evolving rapidly to become a trusted leader in biopharmaceutical solutions.
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With decades of experience in regulatory and quality services, we leverage our global expertise and advanced technologies to provide innovative solutions for the pharmaceutical, biopharmaceutical, and biotechnology industries.
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From drug development to market access, our unified, best-in-class solutions are here to drive your success across the entire product lifecycle.
G&L Healthcare Advisors
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
Printed packaging solutions for clinical trials
and medication adherence
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Smurfit Westrock partners with our customers to
provide printed packaging solutions for their
Clinical Trial and Adherence focused CR-SF
packaging needs. We offer a complete range of
innovative packaging including multi-vial and
injector cartons, complex calendarised blister
packs, and SMART electronically enabled
platforms. Our business is packaging but our
strength is developing solutions to meet your
requirements. We focus on innovation and
leverage our extensive knowledge of the clinical
trial and drug launch process to create package
solutions that optimise supply chain whilst
improving patient adherence. This is what our
customers have come to expect and value
– and this is what we commit to deliver.
Smurfit Westrock
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
Acnos Pharma provides clinical supply services to companies around the globe. Whether it is a comparator, reference drug, co-medication, rescue therapy, or controlled drug you require, Acnos Pharma are ready to meet your demand with innovative solutions.
Acnos Pharma
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
Exhibition Partners
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
DISTILL is a DIY, Drag & drop EDC, flexible, fully compliant, quick and easy to set-up. All for a very attractive budget.
Great fit for pharmas, biotechs, academia, non-profit. For all phases and TA.
Perfect partner for CROs to complete their EDC offering with a mature product that will match their customers small budget.
DISTILL Technologies
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
The companies of Eurofins Clinical Trial Solutions provide a seamless solutions-based approach in support of phase I to IV clinical trials with a unique analytical testing portfolio for Central Laboratory Services, Bioanalytical Services and complex Biomarker Assay Development and Testing Services for drug and vaccine development.
Eurofins Clinical Trial Solutions
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
We help pharmaceutical companies and healthcare professionals access treatment for patients in need worldwide.
As a specialized service partner with expert teams across the globe we:
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Provide global comparator sourcing solutions and services for clinical trials
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Facilitate early access and unlicensed medicines programs
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Distribute licensed medicines worldwide
Inceptua
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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
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
Novotech
Founded in 1997, Novotech is a global full-service clinical Contract Research Organization (CRO) focused on partnering with biotech companies to accelerate the development of advanced and novel therapeutics at every phase.
Recognized for its industry-leading contributions, Novotech has received numerous prestigious awards, including the CRO Leadership Award 2023, the Asia Pacific Cell & Gene Therapy Clinical Trials Excellence 2023, the Asia-Pacific Contract Research Organization Company of the Year Award since 2006.
The Company offers a comprehensive suite of services including laboratories, Phase I facilities, drug development consulting, regulatory expertise, and has experience with over 5,000 clinical projects, including Phase I to Phase IV clinical trials and bioequivalence studies. With a presence in 34 office locations and a dedicated team of 3,000+ professionals worldwide, Novotech is a trusted end-to-end strategic partner of choice.
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
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.
SuperNOVA Clinical Research: Empowering Biotech Excellence
Unleash the full potential of your clinical operations with SuperNOVA Clinical Research. Our comprehensive services include:
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Centralized Clinical Trial Imaging Core Lab & Radiology Services
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Clinical Operations & Project Management
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Quality Assurance (GxP, ISO, Inspection Readiness)
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CRO and Sponsor Staffing
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Policy, Risk Management, Compliance, and Governance
Partner with us to turn your vision into measurable results. We offer white-glove, agile, value-driven, and cost-effective solutions with full-service CRO and imaging capabilities.
SuperNOVA Clinical Research
​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
Taikun Pharma Services is an expert in global clinical packaging, storage and distribution services. Whether it's optimizing flexibility in clinical supply timelines or assisting with regulatory guidelines and packaging design, Taikun Pharma Services is committed to delivering client centric solutions to support the success of clinical trials globally.
Taikun Pharma Services
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
Voiant
MedQIA, WorldCare Clinical and DARC, have come together to form Voiant, the industry’s leading clinical trial imaging solution provider with unparalleled scientific and clinical domain expertise. Voiant’s unique AI-based software platform integrates all aspects of clinical trial imaging, providing biopharmaceutical companies with high-speed delivery of quality clinical endpoint data.
Associate Partners
AI Clinical Research is your trusted partner for personalized, full-service clinical trials in phase I-IV. With global reach, rich expertise, cutting-edge technology, including a Phase I/BE unit and dedicated bioanalytical lab (a unique facility located in Romania), we streamline the journey from trial design to patient recruitment – top quality at appealing costs!
AI Clinical Research
BioBridges
PharmAlliance engages biotech sponsors and CROs with fully vetted contract pros as follows:
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* BioBridges: Commissions nine functional areas of fractional (full and part-time) clinical trial research professionals.
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* Monitor-For-Hire: Provides 4000+ seasoned and fully vetted global CRAs for our partners who seek efficiency and readiness in clinical monitoring.
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* CHEORS: Conducts Cutting-edge health economic insights, economic modeling, country adaptations of the economic models for HTA submissions, systematic literature review,
meta-analysis, and database analysis. Ultimately assisting pharmaceutical companies with
market-access planning and support in payers to modify economic models for evaluating
value-based contracts.
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
CTM is a global, full-service patient recruitment and retention company providing data-driven solutions for almost 30 years. With tailored, in-house services and a full suite of proprietary technology, CTM delivers patient-centric strategies that consistently meet and exceed projections.
CTM
​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
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
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ICON is the world's leading clinical research organisation, powered by healthcare intelligence. From molecule to medicine, we advance clinical research providing outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We develop new innovations, drive emerging therapies forward and improve patient lives.
With 10+ years of patient recruitment expertise in rare diseases, oncology, CNS, and pediatric studies, Patiro offers a flexible, pay-per-enrolled-patient model. With local medical teams in 40+ countries, Patiro deliver personalized, diverse, and ethical recruitment up to 40% faster. Patiro guarantees fully transparent and adaptable services for successful trial outcomes.
Patiro
Clinical trial sponsors should be able to locate independent clinical trial monitors (CRAs) anywhere in the world, FAST. MonitorForHire.com is a patented web-based resourcing tool with over 4,000 registered and pre-qualified monitors in 60 countries including the North American, Latin America, UK, Europe, Asia & MENA.
MonitorForHire.com
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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
Seascape Clinical’s tech platform, ClinOps Pro, helps sponsor clinical operations teams eliminate their busy work (manual, repetitive tasks).
Clients have enjoyed these benefits:
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Lower and streamlined workload, resulting in decreased hiring rate
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Standardized clin ops execution across the entire org
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Less reliance on CRO's reporting
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Faster reporting of trial metrics and risks to senior management by the study team
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Alignment of the entire clin ops “stack”: senior management, program management, and the study team
Seascape Clinical
Stiris Research is a full-service, Clinical Trial Management company specialized in conducting Phase I through IIIB trials. We are the only CRO that was formed from listening to the stakeholders engaged in clinical trials, identifying their unmet needs, and developing a unique, value-based approach to address those needs.
Stiris Research
Trialbee is revolutionizing the patient recruitment ecosystem with technology, people, and passion. Featuring the Honey Platform™ to centralize and standardize your funnel, Precision Recruitment for hyper-targeted digital outreach, medical secondary screening for pre-qualified referrals, and our curated Omnichannel Network, Trialbee helps you take control of your global patient recruitment.
Trialbee
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TrialHub is a clinical data intelligence and feasibility platform, powered by Gen AI.
We’re the first platform to combine country, site, and patient feasibility, as well as automate SoC research and connect reimbursed drugs to indications, in over 70 countries.
Instead of fixing clinical trial challenges, we deliver clinical insights, based on real-time and historical data, to help our users prevent and predict them.
TrialHub
Vita Global Sciences
Vita Global Sciences, a niche talent provider for the life sciences industry, specializing in Clinical Operations, Clinical Development, Quality Assurance, Regulatory Affairs and Biometrics. We address global talent gaps with precision recruitment, streamlined operations, and expert talent care, empowering clients to access crucial expertise for breakthrough treatments and market-defining products.