Meet The Team
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.
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.
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.
We make RBQM simple.
OPRA is our RBQM platform. It delivers easy-to-use Risk Management and Central Monitoring. Built around your processes, it does the hard work for you. OPRA gives you better trial quality, decision making, and efficiency. All resulting in safer patients, compliant trials, and a happier team.
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.
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.
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.
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.
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.
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
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.
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.