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.

Allucent is a Contract Research Organisation that focuses on small and mid-sized biotech. Designed to serve smaller companies, Allucent offers capabilities and expertise that mirror those of larger CROs, but delivered with a more personal and flexible style tailored for the client. Working collaboratively, Allucent stays close to the science that drives therapeutic innovation.

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

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.

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.

CROss Alliance® is a regional, family-owned clinical CRO based in Canton Ticino, Switzerland, operating since 1996. CROSS owns a high standard, Phase I unit (FDA & Swissmedic inspected) for healthy volunteer studies, the oldest private facility active in Switzerland.

For high-risk, hospital-based studies, CROSS has maintained a close collaboration with the Medical University of Vienna for more than two decades. Additionally, for PoC and Phase II studies, strategic partnerships across Central and Eastern Europe have been established.

Beyond the setup and conduct of Phase I BA/BE studies, our main areas of expertise include Anaesthesiology, Gastroenterology, Fertility, Gynaecology, Pain, Dermatology, Ophthalmology, Rare Diseases, and some other therapeutic fields.

Our mission is to deliver tailored and high-quality services, consistently adapted to each client and trial requirements

As a long established and highly respected CRO, the Data Magik team is able to utilise all its experience, as well as the latest technology, to undertake even the most complex of Clinical Research projects in the most efficient manner.

We are a small and friendly team and take pride in developing a strong relationship with our clients. The team all work closely together and span across divisions including Data Management, Statistical Consultancy, Statistical Programming, Quality Control, and Software Development.

We do not believe that there is a ‘one size fits all’ approach to clinical trials, and so we always provide a tailored, specialised solution that meets the specific demands of your trial.

We significantly reduce not only conduct times of individual clinical trials, but also those of drug development programs for our customers.

We are a specialized service provider in the field of Clinical Data Management and have been working successfully for many years with customers from the pharmaceutical industry, with medical professionals in research as well as with external contract research organizations.

Esculape focuses on providing independent data management with a holistic view of your data and the success of your study.

For example, we support the CRO selection, accompany the study set-up and take care of the data integrity and quality in your studies from the beginning to the end of the study.

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.

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.

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.

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.

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.

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.

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.

A premier consulting firm, founded by a team of accomplished and credentialed professionals, will soon debut with a singular purpose—to reduce the complexities of local laboratory data management in clinical trials. With deep industry expertise and a rigorous commitment to quality, we aim to deliver precision-driven solutions that optimize workflows, ensure compliance, and elevate data integrity throughout the trial lifecycle.

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.

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!

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.

OCS Life Sciences is a specialist CRO that supports the full clinical data lifecycle, from biostatistics, CDISC-compliant data management, and submission readiness to real-world evidence, system integration, and managed services. As a long-standing SAS Reseller Partner since 2008 and SAS EMEA Solution Partner of the Year (2024 & 2025), we are a leading provider of SAS solutions with deep expertise in deploying, integrating, and maintaining SAS environments. Leveraging SAS Analytics alongside R and global regulatory standards, we deliver high-quality, compliant data and efficient, future-proof processes. Services are delivered flexibly via resourcing, CRO-led projects, or fully managed service models, so you focus on the science, while we keep the data flowing and the results coming.

P95 is a leading global provider of comprehensive clinical trial services, epidemiology, and real-world evidence (RWE) solutions, with a specialized focus on vaccine development and infectious diseases. Headquartered in Belgium, with regional hubs in Africa (South Africa), Latin America (Colombia), North America (USA), and Southeast Asia (Thailand), P95 operates on five continents, providing tailored clinical research solutions across 40 countries.

Our commitment to flexibility, client focus, and excellence drives us to deliver solutions that make a meaningful impact on public health worldwide.

Founded in 2011, P95 offers full-service CRO capabilities, including clinical operations, study design, data management, and biostatistics. Our mission is to be the world’s favored partner in the field of clinical research and epidemiology in support of vaccine development and use. With 300 staff and over 25 years of collective experience, P95 serves clients ranging from non-profit organizations to pharmaceutical and biotech companies throughout all stages of clinical development and post-marketing.

As part of our growth strategy, P95 has made strategic acquisitions, including Pallas Health Research and Consulting (2021), OnQ Research (2023), 4Clinics, and Assign DMB (2024), enhancing our service portfolio and strengthening our expertise in data, analysis, and writing.

P95 has been a key partner in multiple Innovative Medicines Initiative projects, including ADVANCE, DRIVE, VITAL, and COVIDRIVE, and has supported the European Commission’s Scientific Panel for Health. We are coordinating the largest public-private partnership in Europe to collect ID surveillance information and vaccine effectiveness data (id.DRIVE).

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.

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.

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.

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.

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.

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.

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.

TFS HealthScience is a full-service, global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies to advance innovative treatments and improve patient outcomes.
We combine scientific, academic, and operational understanding with the right people, mindset, and capabilities. Our solutions-driven professionals consistently deliver quality outcomes, on time and on budget.
With nearly 700 professionals across 50 countries, TFS and its strategic partners provide tailored strategic resourcing solutions and clinical development services. Our teams are therapeutically aligned across Internal Medicine, Neuroacience, Oncology, Dermatology and Ophthalmology, With our team being based across Europe and the US, we are able to support any project from the most convenient location.

Veramed is a Clinical Research Organisation (CRO) that provides expert data management, biostatistics and programming services to the pharmaceutical and biotech industry. With precision, consistency and an unwavering commitment to quality, Veramed is dedicated to setting the highest standards for biometrics in clinical trials.

Founded in 2012, Veramed has always been guided by quality, integrity and humanity. This means a culture that genuinely cares for its employees, and employees that genuinely care about the work they do, enabling unparalleled collaboration for industry-leading delivery.

Veramed’s growing team of expert data managers, statisticians and statistical programmers supports analysis and consultancy of Phase I-IV clinical trials across a variety of therapeutic areas. Whether it’s long-term partnerships or rapid-fire project work, Veramed works as an extension of clients’ teams, driving efficient, dependable outcomes.

A truly global CRO, Veramed is headquartered in Twickenham, England, with offices across the UK, Europe, US and India. Veramed is proud to be B Corp Certified ®, committed to integrity and impact in everything we do.

Our vision: We exist to set the new standard for biometrics. By making the right decisions – for our employees, for sponsors, and for patients – we’re redefining what biometrics can deliver in clinical trials.

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.

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.