AdWare Research was established in 1997 as a pre-clinical and clinical data-management and biostatistics provider company. It is a Hungarian family-owned SME.
From the starts AdWare operates according to the highest standards and provides its services in accordance with the international regulations. The activities of the company were broadened in 2002 by developing high quality data management software in order to provide comprehensive opportunities to our partners.
With its in-house developed software (called Mythos) – that is in compliance with 21 CFR Part 11 FDA, and fulfils the criteria of Hungarian and international standards – AdWare ensures the outstanding informatical background of its works.
AdWare applies CDISC standards.

Web: https://www.adwareresearch.com

Services: Data Management, Statistics, Software (EDC)

Setting a new standard in biosimilars

Alvotech is a fully integrated specialty biopharmaceutical company focused exclusively on development and manufacturing of high-quality biosimilar medicines.

Who we are

We are specialists in biopharmaceutical product creation, all along the value chain from cell line development to commercial manufacturing. Our common goal is to be a global leader in the biosimilar space and to deliver high quality cost competitive products to patients worldwide. We come from all around the world, bringing literally thousands of years of combined knowledge and expertise to our mission.

Fully in-house R&D and manufacturing provide:

Cutting-edge in-house R&D capabilities, from cell line, process and product development through process scale-up and manufacturing are completed by a fully integrated clinical and regulatory function, allowing a smooth transition from development through global launch and commercial manufacturing.

State-of-the-art facility for drug substance and drug product manufacturing of biologics, complimented by QC laboratories.

Robust manufacturing processes such as single use-technology, reducing the need to clean and sterilize equipment and allowing flexibility and multiproduct manufacturing.

What we do

Our vision as a company is to build a leading global biopharmaceutical company, while focusing on the development and commercialization of biosimilar medicines for the treatment of severe and chronic conditions, that improves the quality of life for patients around the world.

Web: http://www.alvotech.com

Anju is a customer-first organization providing adaptable life science solutions for clinical research, medical affairs, and data science. TrialMaster, IRMS MAX, and TA Scan, the company’s flagship products, reduce complexities in the drug and device discovery and commercialization process allowing our customers to enhance the quality of their patients’ lives.

Customer First
Our mission is to always be a customer-first organization, powered by a passionate team, providing best-value life science solutions paired with an excellent customer experience to simplify the complexities of life science information management.

Driving Impactful Results
Anju solutions are used by large, mid-sized, and small pharmaceutical companies, clinical research organizations (CROs), and medical device companies as well as full-service medical marketing, market research, and communications agencies. Our technologies facilitate data flow between our solutions and seamless communication with third-party systems, providing a unique opportunity for our customers to leverage critical information and drive impactful results.

Web: https://www.anjusoftware.com/

Services: Data Management, Software (EDC), Software (other)

At AstraZeneca we have transformed our pipeline and returned to growth and, as a result of continued pipeline delivery and commercial execution, we are now entering a new stage of our journey. This is focused on enhanced innovation and the delivery of life-changing medicines that that contribute value to patients and society.
The fundamentals of our strategy are clear. We focus on innovative science and leadership in our three main therapy areas: Oncology; Cardiovascular, Renal and Metabolism; and Respiratory diseases. Backed by a global presence, with strength in Emerging Markets, particularly China, we have a portfolio of specialty and primary care medicines.
At the same time, the world around us is changing and the burden of disease is increasing. We are responding by increasing our focus on growth through innovation – being more patient-centric, doing more with technology, digital and data, and advancing more cutting-edge science.

Web: https://www.astrazeneca.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory

A Global Technology Services organization providing Clinical Analytics and Analytics Engineering services to the pharmaceutical industry

Web: https://www.atorusresearch.com/

Services: Data Management, Statistics, Software (other), Contract Staffing

Bioforum is an innovative, data-oriented Clinical Research Organization (CRO) providing unique, high-quality, tailored solutions for efficient collection, standardization, and reporting of clinical data.

Web: https://www.bioforumgroup.com/

Services: Data Management, Statistics, Medical Writing, Project Management, Software (other)

We have been transforming lives in healthcare since 1885. Our 53,000 employees in 130 markets create value through innovation by infusing long-term, sustainable thinking into our Human Pharma and Animal Health units.

We acknowledge the deep and complex ways the lives of humans and animals are interconnected and work on breakthrough therapies and co-create solutions that help millions of people worldwide live longer, healthier lives.

Web: https://www.boehringer-ingelheim.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory

We want survival in the UK to be among the best in the world. We’re focusing our efforts in four key areas – working to help prevent cancer, diagnose it earlier, develop new treatments and optimise current treatments by personalising them and making them even more effective.

We’ll continue to support research into all types of cancer and across all age groups. And we’re keeping our focus on understanding the biology of cancer so we can use this vital knowledge to save more lives.

We’re increasing our research in key areas such as early diagnosis, and hard-to-treat cancers including lung, pancreatic, oesophageal cancers and brain tumours.

We’re developing new tests, surgery and radiotherapy techniques, and cancer drugs. We want to personalise prevention, screening and treatment and bring benefits to patients sooner.

To help accelerate progress, we’ll be investing an additional £50 million a year into new funding schemes for our researchers. These will encourage collaboration and innovation, and support research tackling some of the biggest scientific challenges in cancer research.

Smoking is the biggest preventable cause of cancer and we’ll work towards the day when no one in the UK smokes – in particular by protecting children and helping people to quit.

We’ll campaign for the best cancer services in all parts of the UK, and give more people the chance to join the fight against cancer.

But we can’t achieve our mission alone. We rely on our dedicated scientists, doctors and nurses, and the generosity of our supporters across the UK. With your help, we can beat cancer sooner.

Web: https://www.cancerresearchuk.org/#/

The CCTU was established in 2011 to lead studies that translate the extensive scientific advances provided by Cambridge Science into clinical application. CCTU is a fully registered CTU and is hosted at CUH as part of the Cambridge BRC.

Web: https://cctu.org.uk/

Services: Data Management, Statistics, Monitoring, Regulatory

Web: http://www.clinfidence.com

Services: Data Management

The Clinical Informatics Research Unit (CIRU) operates as an applied research and enterprise unit within the Faculty of Medicine at the University of Southampton. We provide clinical research solutions and services across the globe which advance data excellence, data quality, data management and improve research methods. Just some of the countries we work with include the United Kingdom, New Zealand, Canada, Belgium, South Africa and more.

Our Lead products are EDGE, our Research Management Programme and CORE for Clinical On-demand Research.

EDGE is a global clinical research management system which is embedded into the clinical research infrastructure across 80% of England’s NHS regions, as well as prominently across Scotland and Northern Ireland. Overseas, EDGE is utilised in Canada, New Zealand, Belgium, South Africa, and India. The EDGE Programme offers a unique approach to the management and conduct of research through purpose-built software and provides research professionals with fast access to real-time data. EDGE enables users to track and manage studies from start to finish as well as providing complete control and oversight of patient and participant recruitment. EDGE promotes collaboration throughout its software and improves methods of working, ultimately resulting in better patient care and treatments.

CORE covers a range of expert services which include the design, build and running of electronic forms used in clinical trials across the UK and overseas, including countries such as New Zealand, Brazil, Switzerland and Turkey. Not only does CORE create the forms you need, it also offers randomisation, data management and provides you with those all-important study statistics. CORE captures vital data for researchers working both in the academic world and commercial setting.

Web: https://www.the-ciru.com/

Services: Data Management, Statistics, Project Management, Software (EDC), Software (other)

Clinion is a global clinical technology company that offers AI-enabled eClinical solutions. ClinionAI consists of EDC, RTSM, CTMS, eCOA and Document Automation that cover the entire clinical trial lifecycle. Clinion is committed to innovating the future of clinical trials through ClinionAI and empowering its partners to manage trials more efficiently at lesser costs.

Web: https://www.clinion.com

Services: Software (EDC), Software (other)

Collective Minds is transforming medical imaging through a global, collaborative platform. Our cloud-based solutions connect healthcare professionals worldwide, driving faster diagnostics, improving patient outcomes, and advancing clinical research and education.

Our GDPR-compliant solutions ensure data privacy and security. Trusted by leading healthcare institutions in over 30 countries.

Web: https://about.cmrad.com

Debiopharm is an independent biopharmaceutical company based in Switzerland with an ongoing commitment to improve patient outcomes and quality of life in oncology and bacterial infections. Our main activities include drug development, drug manufacturing and digital health investment.

Web: https://www.debiopharm.com

The Derby Clinical Trials Support Unit is fully registered by the UKCRC CTU Network. We provide a bespoke service to researchers, sponsors and industry partners – including small and medium enterprises – through the design, delivery, analysis and reporting of high quality clinical research.

Web: https://www.uhdb.nhs.uk/derby-ctu/

Services: Data Management, Statistics, Monitoring, Project Management, Regulatory, Software (EDC), Software (other)

eClinical Solutions seamlessly orchestrates clinical technology and expertise to help accelerate the clinical development process. We provide a spectrum of customized data management services and solutions including EDC, Data Management, Clinical Reporting, and Data Standardization, as well as an innovative Clinical Data Hub platform, elluminate®, which brings advanced visualization and analytical capabilities. Through experience and innovation we empower life science organizations to manage and proactively make decisions regarding clinical trials and programs.

Formed in 2006, the eClinical Solutions team has many years of experience working in the life sciences industry dedicated to clinical data management and programming. The organization was formed to address specific needs that our Leadership team identified through their firsthand experiences, specifically to provide unique and high quality solutions for efficient collection, standardization, reporting and role based utilization of clinical research data. Through a consultative approach and the mindset realizing that each individual organization has a unique set of goals and objectives, we have been partnering with our customers to maximize the use of one of their most valuable assets, their clinical data.

Web: http://eclinicalsol.com

Services: Data Management, Software (EDC)

Eisai is one of the world’s leading research-based pharmaceutical companies. We define our corporate mission as “giving first thought to patients and their families, and to increasing the benefits health care provides,” which we call human health care (hhc). With operations in the U.S., Asia, Europe and it’s domestic home market of Japan, Eisai employs more than 11,000 people worldwide

Web: http://www.eisai.co.uk

EstiMates is a Finnish Contract Research Organization (CRO). Our aim is to bridge science and data and to provide a wide angle to all data related questions.

Our team consists of highly experienced biostatisticians, statistical programmers, data scientists and data managers. We have long-term industry-experience in a extensive range of therapeutic areas and have substantial expertise in all clinical trial phases and academic research.

Web: https://estimates.fi/

Services: Data Management, Statistics, Medical Writing, Contract Staffing

FGK provides full service for clinical studies to biotechnology, medical device and pharmaceutical companies. FGK has the right size to handle international multi-center studies with hundreds of patients or single country studies with a few patients, but is still small enough to guarantee a personal service to the sponsor. Covering all phases and areas of clinical development in Europe, we have experience in every major medical indication. Broad knowledge in rare diseases, ATMPs and Cell Therapy completes our expertise.

Web: https://fgk-cro.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (EDC), Software (other), Data Collection Devices

Frontier Science Scotland is a not-for-profit contract research organisation (CRO) committed to raising the bar when it comes to designing, running and analysing the results of clinical trials. We specialise in data management, biostatistics, and quality services and also offer programming expertise in CDISC models.
We have been established for over 20 years, and bring an extensive track record in working on major international oncology trials, and with a range of commercial and academic partners. Our clients like the fact we are totally independent, passionate about our work, and able to design and deliver bespoke solutions on time and on budget.

Web: https://frontierscience.co.uk/

Services: Data Management, Statistics, Monitoring, Project Management, Regulatory, Software (EDC)

Gilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. We strive to transform and simplify care for people with life-threatening illnesses around the world. Gilead’s portfolio of products and pipeline of investigational drugs includes treatments for HIV/AIDS, liver diseases, cancer, inflammatory and respiratory diseases, and cardiovascular conditions.

Web: http://www.gilead.com

Our Pharmaceutical business has a broad portfolio of innovative and established medicines. We currently focus on developing new medicines in respiratory and HIV/infectious diseases, oncology and immuno-inflammation; with discovery research exploring these and other areas

Web: http://www.gsk.com

We are strategic clinical development experts working with biotech, academic start-ups, pharmaceutical and device companies. Gouya Insights will translate your innovation into a clinical roadmap and design the most efficient clinical development plan. Our experienced and multidisciplinary team provides innovative strategies to meet your clinical milestones and product goals.

Web: https://gouya-insights.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (EDC)

hVIVO, a specialty biopharma company with clinical testing capabilities, is pioneering a human-based analytical platform to accelerate drug discovery and development in respiratory and infectious diseases.

hVIVO changed its name from Retroscreen Virology in April 2015

Web: http://hvivo.com

i2e leads transformation for the life sciences industry through best-in-class analytics and technology solutions. Our market leading execution capabilities, along with expertise in analytics & AI and domain knowledge, help pharmaceutical companies, biotech, and healthcare organizations make clinical trials faster, smarter and easier.

Web: http://www.i2econsulting.com

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (EDC), Software (other), Freelance Data Management, Contract Staffing

The Imperial Clinical Trials Unit (ICTU) sits within Imperial College London as a department within the School of Public Health in the Faculty of Medicine and brings together academic, clinical and trial management expertise from across the Imperial College Academic Health Science Centre. ICTU also collaborates with members of the designated Academic Health Science Network for North West London – Imperial College Healthcare Partners, other national key clinical and scientific opinion leaders, other CTUs and with industry.

ICTU is a UKCRC registered Clinical Trials Unit recognised for its experience and expertise in the development and delivery of clinical trials and associated high quality clinical research projects across a range of therapeutic areas. The unit leads primarily on the design, conduct and analysis of national and international multi-centre trials and the staff, with specialist disease and methodological knowledge, have input at all stages of the trial lifecycle; thus ensuring all activities are conducted according to the principles of ICH GCP and in compliance with the appropriate regulatory and ethical requirements.

Web: https://www.imperial.ac.uk

Services: Data Management, Statistics, Monitoring, Project Management, Software (EDC)

The ICR Clinical Trials and Statistics Unit (ICR-CTSU) is a research-led, academic clinical trials unit (CTU) within the Division of Clinical Studies at the ICR.

ICR-CTSU leads the design, conduct and analysis of phase II and III national and international cancer clinical trials. Our expertise spans the whole clinical trial life cycle and our findings directly influence clinical practice within the NHS and worldwide.

ICR-CTSU clinical trials focus on breast, urological and head and neck cancers, but we also run trials in other rarer cancer types including melanoma, sarcoma and ovarian cancer. We specialise in phase II exploratory and phase III randomised trials of new treatments and technologies (including radiotherapy), and understanding cancer biology and treatment response using biomarker-driven trial designs is fundamental to our research.

We receive core funding from Cancer Research UK, are a UK Clinical Research Collaborative (UKCRC) registered CTU and one of 15 CTUs recognised by the National Cancer Research Institute (NCRI) for professional specialism in the development and delivery of cancer trials.

Web: https://www.icr.ac.uk/our-research/centres-and-collaborations/centres-at-the-icr/clinical-trials-and-statistics-unit

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management

IQVIA is a world leader in using data, technology, advanced analytics and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

Web: https://www.iqvia.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (other), Data Collection Devices, Contract Staffing

At Julius Clinical, science is the foundation. Combined with flexibility, creativity, and innovation, our scientific approach enables fast, efficient, and high quality execution of complex clinical development programs. Our skilled and loyal networks of investigators all around the world allow us to offer superior recruitment in therapeutic area’s such as cardiology, diabetes, CNS and infectious diseases.

Our partners include leading pharmaceutical, biotech, medical device, and food companies, as well as academic investigators. We focus on clinical trials that are likely to have a major impact on medicine and on people’s lives. This type of demanding research requires more than a ‘one-size-fits-all’ approach, and our fusion of scientific and operational expertise enables to deliver results efficiently, on time and budget.

Julius Clinical has on its staff internationally recognised academic leaders who are actively involved in the design, conduct, and interpretation of clinical trials. This scientific expertise and credibility, combined with personal links with peers around the world, means that the company has a truly global reach and reputation. Through our global networks we can quickly select the most appropriate and high-performing sites to take part in a trial, and ensure that investigators are inspired and motivated.

Web: https://www.juliusclinical.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (EDC), Software (other)

As a leading global oncology contract research organization (CRO), Kapadi partners with biopharmaceutical companies, physicians, and institutions to accelerate innovative clinical research. With comprehensive expertise across the entire product lifecycle, we provide custom-curated solutions to support our clients in moving new oncology therapies from concept to commercialization.
Kapadi is a loving and caring individual who puts the needs of others before their own. They possess a strong sense of responsibility and trustworthiness, with high regard for justice and honesty.

Web: http://kapadi.com

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (EDC), Software (other)

LINK Medical is a leading Contract Research Organization and Regulatory service provider offering experts, flexible services, and innovative technologies across Northern Europe and beyond. Additionally, our transparent Nordic culture provides a high-quality service delivery based on respect, work integrity and a strong focus on solutions.

Our in-house team of Data Managers has broad experience across different industries, in all major therapeutic areas and phases of development. We are a Nordic team with global reach that has supported clients in more than 30 different countries. With proven results through over more than 500 eCRF builds completed we are true experts in designing tailormade clinical databases that meet the unique needs of your project. By using the latest technologies for data capturein combination with well-integrated and efficient Data Management processes we secure data integrity and quality, empowering you to make informed decisions. Collaboration is at our core; we seamlessly collaborate with your team to ensure short timeframes for study deliverables.

Web: https://linkmedical.eu

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (EDC), Software (other)

The LCTC is fully registered within the UKCRC registered CTU network. We are within the Faculty of Health and Life Sciences at the University of Liverpool.
We work with the NHS and commercial partners, patients and the public to contribute to the identification and evaluation of new and innovative treatments and devices.

We have particular expertise in personalised medicine, surgical interventions, and re-purposing of and establishing evidence for existing treatments used within the NHS.

In partnership with other trials methodologists we contribute to the advancement of methods to improve the design and delivery of clinical trials.

We support the development of increased capacity for conducting clinical trials locally and nationally by encouraging the development of clinicians, healthcare professionals, and trials methodologists as leaders in clinical trial research.

Web: https://lctc.org.uk/

Services: Data Management, Statistics, Project Management, Regulatory, Software (EDC), Software (other), Data Collection Devices

Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. Celebrating 25 years of ground-breaking technological innovation across more than 35,000 trials and 10 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and the largest patient-level historical clinical trial data set in the world. More than 1 million registered users across approximately 2,300 customers trust Medidata’s seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster. A Dassault Systèmes brand (Euronext Paris: FR0014003TT8, DSY.PA), Medidata is headquartered in New York City and has been recognized as a Leader by Everest Group and IDC. Discover more at www.medidata.com and follow us @Medidata.

Web: https://www.medidata.com

Services: Software (EDC), Software (other), Data Collection Devices

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. Beyond electronic data capture (EDC), Mednet’s solution set provides the tools required to build and manage all types of clinical research, while enabling organizations to adapt to evolving demands and requirements. Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for nearly 20 years to deliver the technology innovation, experience and reliability they need for success.

Our platform, iMednet, is a comprehensive, cloud-based, clinical data management system, centered around a robust EDC and built from the ground up with key native modules, including: Randomization, Trial Supply Management, Adjudication, ePRO, Payments, and DICOM Imaging.

Designed to also allow easy integrations, the platform enables research teams to meet the rapidly evolving requirements of clinical research, while supporting a wide range of study types and designs. iMednet is highly flexible and intuitive, enabling users to get studies up and running quickly, while ensuring easy onboarding of the entire research team and clinical trials sites.

Web: https://www.mednetsolutions.com/

Services: Software (EDC), Software (other)

For more than 30 years, METRONOMIA has been an exceptional partner for biostatistical consulting, biostatistical services, clinical data management and medical writing.

Our team of more than 120 highly skilled and committed experts serves the needs of our customers with the highest degree of flexibility, reliability and quality.

Our clients are pharmaceutical, biotech and medical device companies. Over 650 successful projects in all clinical development phases and major therapeutic areas are a testament to our data science excellence and exceptional service quality!

Web: https://metronomia.net/

Services: Data Management, Statistics, Medical Writing

Our Data Centre Hub is based at the Micron UK office, and from here we can meet all of your data delivery and statistics needs, from initial study design through to statistical analysis and reporting

Web: http://www.micron-group.com

Our purpose: We use the power of leading-edge science to save and improve lives around the world
For more than 130 years, we’ve brought hope to humanity through the development of important medicines and vaccines. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities.

Web: https://www.msd.com/

Our mission is to facilitate human health research and its transformation into medical practice. NIHR BioResource is a unique and powerful resource for studying disease mechanisms and investigating the links between genes, the environment, health and disease, enabling scientific discoveries and facilitating translational medicine for the benefit of patients.

We have over 270,000 consented volunteers with and without health conditions, who are willing to participate in academic and industry-led experimental medicine and clinical research studies. Recruitment is on a national and local level, with local BioResource centres spread across England.

Web: https://bioresource.nihr.ac.uk/

Services: Data Management, Software (EDC), Data Collection Devices

Novotech is a globally recognized full-service clinical research organization (CRO) and scientific advisory partner for biotech and small – to mid-sized pharmaceutical companies seeking to advance drug development. With deep therapeutic and regulatory expertise and an expansive global footprint across the Asia-Pacific region, North America, and Europe, Novotech offers clients an accelerated path to bring life-changing therapies to market.

Web: https://novotech-cro.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (other)

At Nutricia Research we believe that every consumer and patient deserves optimal nutritional support. We use life science, food science and technology, together with the passion, drive and expertise of over 900 employees, to pioneer nutritional solutions for those with special nutritional needs

Web: https://www.nutriciaresearch.com

Our Mission:
Revolutionising clinical trials with tech-driven platforms that harness real-world data to drive innovation and accelerate the delivery of life-changing treatments to market.

What NWEH does:
NWEH develop cutting-edge, technology-driven platforms that harness real-world data to transform clinical trials. Our solutions streamline the entire trial process—from feasibility assessments and optimised trial design to participant recruitment, decentralised trial delivery, real-time safety monitoring and advanced data feeds.
By integrating real-world insights with innovative digital tools, we enhance trial efficiency, improve participant experiences and empower sponsors with data-driven decision-making.
We help bring treatments to market faster through smarter, safer, and true-to-life™ clinical trials.

Web: https://www.nweh.co.uk

Services: Statistics, Project Management, Regulatory, Software (EDC), Software (other)

Orion is a globally operating Finnish pharmaceutical company – a builder of well-being. We develop, manufacture and market human and veterinary pharmaceuticals and active pharmaceutical ingredients. We believe that health and well-being create the foundation for a good life and society. We are continuously developing new drugs and treatment methods.​ We collaborate closely with healthcare professionals and leading global research institutions and pharmaceutical companies.

Web: https://www.orionpharma.com/

PharMarketing GDPR Life Sciences is an operational consulting company based in France and acting in Europe. We help companies to become compliant with Data Privacy European Law EU GDPR (eugdpr.org), with US Privacy Shield, GCP and IT Good Practices (ISO 27001). We also provide Legal Representation in the EU for Clinical Research, for GDPR and deliver Audits Services of IT systems, of business processes, of quality compliance, etc. We are dedicated to organisations in Life Sciences sector manipulating Patients’ Data.

Web: https://www.pharmarketing.net/

Services: Data Management, Regulatory

PHASTAR is a specialist CRO offering statistical consulting and clinical trial reporting services to the pharmaceutical industry. Our number one priority is to ensure the work we produce is of the highest quality: every project PHASTAR undertakes is supervised on methodology and utilises unique internal processes designed to ensure the best quality.

Our aim is to provide a service that is ahead of our competitors: in the last 2 years, we have been involved in the design and reporting of over 200 studies, and each has delivered on-time and with no quality issues.

We can provide data collection as a MEDRIO partner. Talk to us about using MEDRIO for your study – MEDRIO is fully functional, easy to use, and sensibly priced.

Web: http://www.phastar.com

Pierre Fabre Laboratories design and develop innovative solutions in collaboration with partners and health care professionals, constantly drawing its inspiration from nature and plants, always placing the patient at the heart of its research and development (R&D).

Medical R&D’s mission is to respond to unmet medical needs with innovative targeted therapies, that are efficacious, safe and benefit the patient, focused on Oncology, Dermatology and Rare Diseases.

Web: https://www.pierre-fabre.com/en

Services: Data Management, Statistics, Project Management

The PPD™ clinical research business of Thermo Fisher Scientific is a leading provider of global CRO solutions.

We provide comprehensive drug development, laboratory and lifecycle services to customers across pharmaceutical, biotechnology, medical device, academic and government entities. By harnessing innovative technology and expertise, we work to empower our customers to bring therapies to market, faster.

Web: http://www.ppd.com

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory

Our Approach
Continually optimizing our processes to deliver the right mix of agility and knowledge to support our most innovative biotech and specialty pharma sponsors.

What we do
Your compound shows spectacular promise, but it seems there’s an obstacle at every turn – finding hard-to-reach patients, defining relevant endpoints, navigating the regulatory maze, and ultimately obtaining clean, conclusive data.
Our Built for Biotech model is a compilation of the most successful techniques and capabilities observed across our experience, applied to provide a specialized customer experience.

Our approach in action
Therapeutically focused teams of clinical professionals have the knowledge and experience necessary to effectively manage any situation that may arise in your trial. Our approach is firmly grounded in comprehensive project management principles and well-defined processes.

Web: https://premier-research.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Data Collection Devices, Contract Staffing

Traditional CRO push a full-service, “cookie-cutter” agenda, offering little compromise for the small Sponsor; ProPharma’s Research Consulting Organization RCO model leads with strategy to help de-risk programs and create tailored solutions to maximize probability of success.

ProPharma has transformed its organizational structure and solutions to put its clients at the very center. We offer a suite of bespoke consulting solutions across service lines and functional areas of expertise to span the full product life cycle. ProPharma embraces partnerships to reduce delays and drive consistency with dedicated and experienced strategists and program managers for end-to-end oversight.

Web: https://www.propharmagroup.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (other), Freelance Data Management, Contract Staffing

Our mission is to be the greatest CRO in the world as measured by our employees, clients, and sites. We meet deadlines and enrollment milestones, time and time and time again. We listen and anticipate our sponsors’ needs before they even know them. We dedicate ourselves to success on every level of our company.

Simply put, working with us gets you more: More passion. More results. More success.

Web: https://www.psi-cro.com

PureCDM is a leading provider of end-to-end clinical data management and regulatory-compliant technology solutions for the biopharmaceutical and MedTech industries. With over 14 years of global and cross-functional expertise, we specialize in streamlining clinical trial data processes, ensuring compliance, and supporting the development of innovative medical products. By bridging the gap between invention, technology, and commercialization, PureCDM transforms clinical data into a strategic asset, accelerating the path from research to market

Web: https://purecdm.com.au

Services: Data Management, Statistics

At Qlarix, we facilitate the adoption of Risk-Based Quality Management (RBQM) by offering technological solutions developed alongside our clients for the overall light of clinical studies.

We combine research expertise with innovative technology to empower organizations in their journey towards adopting a robust risk management culture.

WiseCLIN, our RIsk-Based Oversihght System, sets the standard for next-generation clinical trial oversight.

Web: http://www.qlarix.com

Services: Project Management, Software (other)

RARAS uses its resources in Latin America to launch development programs minimizing risks and generating robust data that can be used for FDA, EMA, ANVISA and other highly regulated agencies for further funding rounds or registration purposes. From regulatory strategies, to medical writing, trial design and execution including data management we support established companies to startups, from idea to product.

Web: https://rarascro.com

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (EDC)

Globally, Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases and neuroscience. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management. Roche’s personalised healthcare strategy aims at providing medicines and diagnostics that enable tangible improvements in the health, quality of life, safety and survival of patients. Twenty-eight medicines developed by Roche are included in the WHO Model Lists of Essential Medicines, among them life-saving antibiotics, antimalarials and chemotherapy. Roche in the UK employs over 2,000 people in pharmaceuticals and diagnostics

Web: https://www.roche.co.uk

Science4Tech’s mission is to facilitate access to multiple innovations enabled by technology to improve the quality, rigour and a reliable clinical research based on the scientific method, supporting pharmaceutical and biotech companies in the acceleration of drug development to bring much-needed therapies to patients sooner.

Our data-driven solutions aim to improve all stages of clinical trials, under strict scientific rigour and in compliance with the regulatory framework.

Web: https://s4t.health/

Services: Data Management, Statistics, Monitoring, Software (EDC), Software (other), Data Collection Devices

SCOPE International is an independent Full-Service Contract Research Organization (CRO) with a network of 15 local offices and business entities throughout Europe. SCOPE offers a complete range of clinical development and consulting services to the pharmaceutical, biotechnology and medical device industries, and is supported by long established partnerships in other geographies. We focus on providing cost-effective services while achieving industry leading benchmarks in timelines, costs and quality. Our experience and expertise in managing all major indications in clinical phases I – IV makes us the perfect partner for you to work closely together to develop solutions that exactly fit your needs and to guide you smoothly through all development phases. In business since 2000, SCOPE has conducted over 260 studies with 70,000 patients across 30 countries worldwide. At SCOPE we work with people for people.

Web: https://scope-international.online/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory

In July 2015, bioCSL and the influenza vaccines of Novartis joined forces to create Seqirus, now the second largest influenza vaccine company in the world. Cutting-edge facilities, technologies and technical expertise, Seqirus will be a reliable supplier of seasonal influenza vaccine with the ability to rapidly respond to pandemic threats

Web: http://www.seqirus.com

The Southampton Clinical Trials Unit (SCTU) is a UKCRC registered CTU with expertise in the design, conduct and analysis of multicentre interventional clinical trials. We work in partnership with investigators to deliver high quality trials that will directly influence routine clinical practice.

Web: https://www.southampton.ac.uk/ctu/index.page?

Services: Data Management, Statistics, Monitoring, Project Management, Data Collection Devices

Suvoda is a global clinical trial technology company specializing in complex, life-sustaining studies in therapeutic areas like oncology, central nervous system (CNS), and rare disease. Founded in 2013 by experts in eClinical technologies, Suvoda empowers clinical trial professionals to manage the most urgent moments in the most urgent trials through advanced software solutions delivered on a single platform. Headquartered outside Philadelphia, Suvoda also maintains offices in Portland, OR, Barcelona, Spain, Bucharest and Iasi, Romania, and Tokyo, Japan. The company’s Net Promoter Score (NPS) consistently exceeds the technology industry average, contributing to the company being selected by trial sponsors and CROs to support more than 1,000 trials across 80 countries. To learn more, visit suvoda.com.

Web: https://www.suvoda.com/

Services: Data Management, Software (other)

Tecro Research is a niche Data Management and Statistical programming provider. We are committed to delivering quality work in a timely manner through utilizing our unique combination of skills and in-depth knowledge of Data Management, complemented by years of Statistical Programming experience.

We have a wealth of aligned expertise available to us on a collaborative basis, with all our associates having at least 10 years’ experience in their respective fields. As a group, we can offer CRO services ranging from protocol development through CSR writing, including medical writing, data management, statistical analyses, clinical project management, medical and clinical data monitoring, pharmacovigilance and auditing, we are also able to manage specialist vendors on behalf of our clients.

Our business model of collaborating associates ensures a flexible, efficient approach to delivering quality solutions in a cost-effective manner. Quality is assured, not only by the experience of the leadership team and collaborators, but also by the personal ownership of each project by a senior team leader.

Web: https://tecro-research.com/

Services: Data Management, Statistics

At TRI, we implement Risk-Based Quality Management (RBQM) to drive better clinical trials, improve patient safety, and be compliant with Good Clinical Practice (GCP).

Deployed on over 450 clinical trials, we understand the challenges of RBQM and how to overcome them. Our industry-leading RBQM platform, OPRA, is built by operational experts to support Risk Assessment, Risk Management, and Central Monitoring – all in one intuitive system.

With two core modules, OPRA-RAM and OPRA-CM, OPRA enables teams to focus on what matters most, prioritize critical risks, and take confident, timely action – all backed by clear, evidence-driven insights.

What sets us apart? Our operational focus. Whether you need expert support or a seamless tech solution, we’re here to help. With real-world clinical trial experience, our RBQM team provides the guidance you need to meet regulatory requirements (ICH E6/E8) and confidently embed RBQM at the heart of your trials.

That’s why leading global players trust TRI. We’re not called The RBQM Experts for nothing.

Web: https://www.tritrials.com/

Services: Data Management, Statistics, Monitoring, Project Management, Regulatory

Web: https://www.gla.ac.uk/researchinstitutes/healthwellbeing/research/robertsoncentreforbiostatistics/

Services: Data Management, Statistics, Monitoring, Project Management

Founded in 2021, VHypotenuse was born from a deep-rooted passion for science and technology, driven by a strong desire to make a meaningful impact on the world. Originally established as an IT and Data Management company, VHypotenuse has since expanded into the field of Clinical Research, conducting clinical trials across a range of therapeutic areas.

At VHypotenuse, we are committed to delivering innovative and reliable solutions to our clients. Our expertise spans:

Software Development

Clinical Research Solutions

Consulting Services

Biostatistics

Clinical Data Management

Our mission is to bridge the gap between technology and healthcare, empowering organizations with data-driven insights and advanced solutions to improve outcomes and accelerate progress.

Web: https://vhypotenuse.com

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (EDC), Software (other), Data Collection Devices, Freelance Data Management, Contract Staffing

For over 20 years, Vitaflo® has been at the forefront of developing innovative specialized clinical nutrition products for Inborn Errors of Metabolism (IEM), nutrition support and disease specific conditions such as renal disease.
Working in partnership with world key opinion leaders and patients, Vitaflo’s research and development team conducts clinical trials on all our products with leading centers around the world.
Vitaflo’s aim is to create products that combine the best of cutting edge research with the lifestyle demands of modern living, ensuring the most acceptable products are available for the patient.

Web: https://www.nestlehealthscience.co.uk/vitaflo

WriteSource Medical Pty Ltd is an Australian based medical writing and biostatistics consultancy with a global client base. We combine the power of statistics with the ability to communicate them.
At WriteSource Medical, we pride ourselves on providing accurate, ethical and balanced services to the pharmaceutical and academic sectors. We also offer training in biostatistics and medical writing. WriteSource Medical Pty Ltd works closely with you to understand and meet your needs. We comply with relevant industry standards for data management, medical writing and biostatistics.

Our highly qualified team includes biostatisticians, data scientists and medical writers.

Web: http://writesourcemedical.com.au

Services: Data Management, Statistics, Medical Writing, Project Management

The York Trials Unit provides a number of services including study design, randomisation, trial coordination, data management, statistics, economic evaluation and outcomes. We also run a number of courses about clinical trials. More information on both historical and currently active trials can be found in the relevant project microsites

Web: https://www.york.ac.uk/healthsciences/research/trials/

Services: Data Management, Statistics, Project Management, Software (other)

Merative is a data, analytics and technology partner for the health industry. For nearly five decades, Merative has combined trusted technology and deep industry expertise to help push healthcare forward.

Zelta™ is Merative’s clinical trials solutions business that includes both a clinical data management and acquisition platform (formerly IBM Clinical Development), and consulting, enablement and extension services. We believe there is a better way to solve today’s – and tomorrow’s – complex research challenges, and we are enabling these solutions in Zelta. Zelta lets you take full command of every aspect of your clinical trials and research. We offer a truly unified clinical data management and acquisition platform with customizable modules that can be tailored to the meet the unique needs of your clinical trials. From the simple to the complex – we can support your research needs.

Web: https://www.merative.com/clinical-development

Services: Software (EDC), Software (other)