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Meet The Team

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

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

Premium Partners

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TCR-Solutions is a boutique, full service, global Clinical Research Organisation established in 2015 to support Biotechnology, Pharmaceutical and Academic sponsors worldwide.


We help these partners navigate the unique and ever-changing hospital environment, through an unrivalled understanding of the people, processes and priorities involved, while always keeping patients at the heart of what we do.


Our sustained ethos of putting hospital sites at the very heart of what we do means we continue to successfully deliver clinical trials across a wide variety of phases and therapeutic areas. 


Recent highlights include five important and innovative COVID studies; highly complex first in-man studies; multiple oncology, radiopharmaceutical, gene therapy, psychiatry, and ophthalmology projects; as well as post-marketing Real World Evidence programmes. Over the past 18 months, we have also carved out a niche in medical device studies.


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TriloDocs is an AI tool that generates an initial draft of a Clinical Study Report that accurately reflects the source material (protocol, statistical analysis plan, data tables and figures). The tool not only creates formatted tables and figures but also meaningful text around them, highlighting clinically relevant findings with no risk of hallucinations or ‘making things up’. The medical writer and the clinical team have a first draft to discuss in a matter of days instead of weeks. The tool is unique – created using over 100 years of medical writing experience.

TriloDocs is created by medical writers for medical writers.


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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 Protec4on 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.


Content 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


An efficient and effective clinical supply chain strategy can provide a huge added-value to a pharma/biotechcompany running a drug development program. With a proper demand and supply strategy, an optimized clinical supply chain will shorten the production timelines, significantly reduce the risk of patient drop-off, improve clinical trial timing, and cut the budget.

At Boostcode, we have more than 20 years of expertise in all aspects of the supply chain across multiple industries, with a focus on pharma and biotech. In recent years, we focused our activities on the support to biotech companies wishing to transform their clinical supply chain.



PHARMExcel is an award-winning, full-service Contract Research Organisation (CRO) providing a flexible and innovative approach to clinical trial delivery. The company is recognised for its in-depth knowledge and experience of the clinical research environment, particularly in the UK, and has a network of regulatory and industry associates, allowing it to provide a global reach.



Premier Research, a clinical research company, is dedicated to helping biotech, specialty pharma, and device innovators transform life-changing ideas and breakthrough science into new medical treatments.


As a global company, Premier Research specializes in the use of innovative technologies for smart study design and trial management to deliver clean, conclusive data to sponsors.


Whether it's developing product lifecycle strategies, reducing clinical development cycle times, securing access to patients, navigating global regulations, maximizing the impact of limited rare disease data, or providing expertise in specific therapeutic areas, Premier Research is committed to helping its customers answer the unmet needs of patients across a broad range of medical conditions.

Premier Research

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OPRA, our platform, enhances Risk-Based Quality Management (RBQM) by offering integrated Risk Management, Centralized Monitoring, and Subject Monitoring. It seamlessly automates tasks, improving trial quality, decision-making, and efficiency. Subject Monitoring ensures close oversight of patient data, enhancing safety and compliance, and contributing to team satisfaction. OPRA streamlines trial management, upholding high standards for patient well-being and trial success.

Triumph Research Intelligence


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.



Printed packaging solutions for clinical trials

and medication adherence

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.


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

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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Alderley Analytical is a Contract Research Organisation (CRO) specialising in Regulatory Bioanalysis.  Our GLP and GCP accredited laboratories specialise in analysing plasma, blood, urine, or other tissue samples to detect and quantify the drug or biomarker in the sample, for your pharmacokinetic, exposure and biomarker endpoints.     Whether your drug is a small molecule, peptide, oligonucleotide or large molecule we have the technology and expertise to support your project.

Alderley Analytical

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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



ESMS Global is a niche service provider offering 24/7 emergency medical response services for Clinical Trials and Medical Information.  

With global contracts across 80 countries, speaking 45 languages, our background and culture is built on providing support in emergency situations. We focus on patient safety creating a reliable and robust solution for your business. 


Clinical Services International

Clinical Services International (CSI) provides the most comprehensive solutions to clinical trial supplies including sourcing of medicines and devices, distribution and all services needed for successful conduct of studies.

We have offered our solution to more than 1000 clinical trials all over the world.


Headquartered in London and with operations in 5 continents, we provide efficient solutions to the most complex adaptive trials worldwide.

We accelerate drug development and reduce timelines by providing a fully integrated service.

  • Address Regulatory, Quality, Operational, Clinical Requirements, and Forecasting

  • Manage the entire supply chain and offer tailor-made solutions 

  • Comprehensive expertise in Oncology and Biosimilar products

  • Direct access to all major Pharmaceutical Manufacturers and more than 95 audited suppliers globally. 

  • Trusted partner of leading Biopharmaceuticals, CROs and CMOs.


Complex innovative clinical trial designs require an integrated synergetic approach to assess novel drug compounds for safety and effectiveness which often span esoteric, regulated and safety outcomes in all phases of the drug development life-cycle.

The companies of Eurofins BioPharma Services 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 BioPharma Services


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

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.



Through nationwide phlebotomy and sample collection services, flexible health assessments and expert laboratory testing, Inuvi creates certainty in the worlds of population health studies, clinical trials, and mass testing.

From simple phlebotomy to more comprehensive health assessments, Inuvi’s nationwide network of Health Practitioners is on hand to support your project, anywhere, anytime.

Our state-of-the-art, UKAS accredited medical laboratory delivers expert testing and diagnostic services. From biochemistry to virology and microbiology we provide a fully comprehensive range of tests, empowering you with an accurate picture of your population’s health.

Together, we’re fuelling healthier futures.




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.

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Intelsius has been designing and manufacturing environmentally sustainable and regulatory compliant sample transport and temperature-controlled packaging for 25 years.

As well as offering a diverse range of sample transport and temperature-controlled packaging solutions, our expert Technical Services team and ISTA-certified laboratory ensure we can design, test and qualify your packaging with your specific payload and shipping lane in mind.


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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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Precision medicine is in our blood, our cells, our genes, and our name. Precision for Medicine, the full-service global CRO, is purpose-built to accelerate clinical research and development processes to bring life-changing therapeutics to those who need them most. We integrate clinical operations excellence, laboratory expertise, and advanced data sciences to deliver on the promise of personalized therapy; translating research into real-world results and forever reimaging how to get there.

Precision for Medicine

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RSSL is a world leader in providing quality scientific analysis, research, consultancy and training solutions to the global Life Science sectors. Supporting all phases of clinical development through to commercial release


From our state-of-the-art MHRA and FDA approved facilities, our multi-disciplinary team work collaboratively with clients to develop drug products that are safe, innovative and capable of transforming lives around the world.


Associate Partners


APICES is a full-service CRO with offices in Spain and France and capabilities to cover all Western European countries. APICES has deep experience in oncology, hematology, and all other therapeutic areas and provides a wide range of clinical research and development services, from project design to publication of results. Flexibility, Excellence and Client Satisfaction are our key drivers since 2009 proven with > 50 public acknowledgements in scientific journals to date.



Biopharma Group

Biopharma Group’s highly experienced team provides comprehensive CDMO services from R&D and consultancy solutions for lyo and liquid formulations to fill-finish GMP clinical manufacturing (phase 1 & 2) to the pharmaceutical, diagnostic and biotech industries.

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Keosys Medical Imaging is a central imaging lab providing medical image management and reading services to biotech and pharma clients around the world. Keosys can handle CT, MRI, PET, SPECT and X-ray scans for your clinical trials and has its own team of developers to quickly manage new imaging criteria.

Keosys Medical Imaging


Lumis Life Science Consulting GmbH is an independent subsidiary of Lumis International GmbH to provide customer-tailored consulting and solutions for regulatory consulting and Services, clinical trial oversight and vendor management and quality management. Jointly with our customers, we develop tailored solutions to optimise their clinical development program. We collaborate with a network of experienced subject matter experts, cooperation partners, and consultants.

Lumis International


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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OPIS was founded in 1998 by medical doctors from the Pharma Industry and is a Global clinical CRO with 25 years of experience in a wide range of therapeutic areas. OPIS provides full-service, 360° clinical trial support from study concept creation and protocol development to full project execution, study data handling and up to study closure, analysis, and reporting.


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Optimapharm is a globally operating, leading, mid-sized, full-service CRO aiming to deliver new therapies to improve and save patients’ lives. 


Optimapharm conducts phase I – IV studies in all therapeutic areas, including complex medical device studies.

With 26 strategically located offices, Optimapharm is giving unrivalled access to patients and investigators worldwide. 


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PCI is a leading global CDMO, providing clients with integrated end-to-end drug development, manufacturing and packaging capabilities that increase their products’ speed to market and opportunities for commercial success. PCI brings the proven experience that comes with more than 90 successful product launches each year and over five decades in the healthcare services business. Leading technology and continued investment enable us to address global drug development needs throughout the entire product life cycle – from manufacturing capabilities through the clinical trial supply chain and into commercialization.


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Pro-ficiency is a next-generation learning engine for clinical trials. This custom, online, protocol-specific training can help to boost site performance, optimize enrollment, and improve protocol compliance and execution. Pro-ficiency is redefining the learning outcomes learners and leaders should expect from your training investment.



Randox Health

Following decades of pioneering research and development, Randox Health offer clinicians and physicians an unrivalled range and combination of tests to facilitate effective disease management, screening, and treatment, with over 1,200 tests in our portfolio, white-labelled health checks, and phlebotomy services.

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TFS HealthScience, a global CRO, collaborates with biotech and pharma firms worldwide in their clinical development. With 800 experts, we offer tailored research services in 40+ countries. Providing full clinical development, strategic resourcing, and solution-driven teams, TFS works for a healthier future, aiming to expedite treatments for patients.

TFS HealthScience


Thriva Solutions

Thriva Solutions is a UK-based HealthTech company that offers a remote diagnostic testing platform and services to help clinical studies become more diverse, accessible, and secure. We are revolutionising the diagnostics industry by offering innovative testing solutions that are flexible, scalable and convenient. We aim to provide a human-centric experience and focus on diversity, accessibility, and accuracy. By working with Thriva, you can be a part of a robust and impactful scientific future

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