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Meet The Team

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COG New England

For more information on sponsorship opportunities, please contact Alex O’Leary. 

Email: | Phone: +44 (0)7795 345 108.

Premium Partners


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.


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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

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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.


Content Partners

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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:

  • Clinical supply management

  • Integrated formulation development, clinical manufacturing & blinding

  • Specialty handling (potent, cytotoxic, controlled)

  • Direct comparator/reference product sourcing

  • Clinical packaging/labeling

  • Extensive clinical storage, cold chain capabilities & global distribution

  • Demand-led supply

  • Direct-to-patient solutions

  • Clinical returns, reconciliation & destruction

Catalent Clinical Supply


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

Delve Health


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


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. 


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Clinical trial sponsors should be able to locate independent clinical trial monitors (CRAs) anywhere in the world, FAST. 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.

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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.


Recruitment Partner

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.

RBW Consulting

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Exhibition 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


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.


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Axiom is celebrating over 22 years of delivering hundreds of studies in dozens of countries. Since its founding in 2001, Axiom has delivered data-driven, powerful, and cost-effective eClinical Solutions and Services dedicated to small-to-medium life science companies. Axiom Fusion eClinical Suite is the most adaptable, Unified Platform that serves as the Connected Hub for all your Clinical Trial and operational data and reporting. Choose from 15+ unified modules on a single platform: EDC, DM, RTSM/IRT, CTMS, Inventory Management, ePRO, eConsent, Patient Portal, AE/SAE Tracking, Safety Database, Central/Local Lab, Imaging Management, eTMF, and 24/7 Project and Clinical Data Reporting. We are an embedded partner dedicated to the success of your study, offering managed services such as: Data Management, On-Demand Data Analytics, Biostatistics, Clinical Management, eTMF Management and Pharmacovigilance.

Axiom Real-Time Metrics


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

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.


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Ancillare fully manages, medically advised ancillary supply and equipment programs for global Phase I-IV clinical research with corporate offices in the US and the Netherlands, and distribution hubs in Argentina, Australia, Brazil, Canada, China, India, Israel, Japan, Korea, Mexico, Philippines, Taiwan, Turkey, and United Kingdom.



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

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Harbour Clinical

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:

  • Quality Assurance (Inspection Readiness, site/vendor audits, etc)

  • Vendor Oversight

  • Clinical Operations

  • Data Management

  • Programming

  • Biostatistics

  • Medical and Safety Management

  • Medical Writing

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.



Illingworth Research Group provides mobile research nursing and patient concierge services supporting patient enrollment and retention in decentralized trials. We are the longest established mobile home nursing provider with 20+ years of experience, offering our services in over 45 countries globally. Illingworth brings the patient to the trial and the trial to the patient.

Illingworth Research

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MLM Medical Labs

MLM Medical Labs is a global leading specialty and central laboratory with comprehensive research services and analytical capabilities in Europe and North America. Offering standard and fully customizable biological specimen testing and auxiliary logistics services across a wide spectrum of therapeutic areas from nonclinical and preclinical through phase IV clinical trials.

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Sharp Clinical

Sharp Clinical provides a complete range of clinical services from the pre-clinical stage through to commercialization. Our project management and operational teams have vast experience in managing local and global

clinical trial supplies for a wide variety of dosage forms and innovative treatment candidates, including orphan drugs and gene therapies.


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


SuperNOVA Clinical Research: Empowering Biotech Excellence


Unleash the full potential of your clinical operations with SuperNOVA Clinical Research. Our comprehensive services include:


  • Centralized Clinical Trial Imaging Core Lab & Radiology Services

  • Clinical Operations & Project Management

  • Quality Assurance (GxP, ISO, Inspection Readiness)

  • CRO and Sponsor Staffing

  • 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


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.




VCTC is the UKs first and only clinical trial site established specifically to address the burden that participants face when taking part in clinical trials. Our virtual and decentralised trials place the participant and the centre of their trial experience, providing them with more control over how, when, and where they choose to participate.



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

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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

  1. create, send and receive proposals on the cloud and

  2. 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.



At Median, we transform medical images into meaningful, actionable insights to help better diagnose, treat, and monitor patients. Median’s Imaging CRO business provides best-in-class clinical trial imaging solutions for oncology studies, empowering our life sciences partners to accelerate the development and delivery of life-saving cancer treatments with unmatched operational excellence and reliability. And we don’t stop there. We are forging the way when it comes to innovative imaging technology, leveraging the latest in AI-powered imaging intelligence to develop actionable insights for sponsors worldwide.


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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


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.



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.


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