Corporate Membership of the Association for Clinical Data Management was recently launched. For a fixed annual subscription the corporate membership allows you to obtain the following benefits:
recognition as a Member Company of the ACDM
unlimited number of individual ACDM members at a single location of your organisation
add/remove members using our online Membership Management Area
reduced prices for attending training courses and the Annual Conference
free online listing of your organisation on the ACDM website
Founded in 2013, Algorics is a specialized data solutions partner to the clinical research and life sciences industry focusing on data management, biostatistics, programming, and data standardization. Driven by our next-generation technology suite – MetaVate and Clarity, an innovative solutions platform and a highly experienced team, we provide end-to-end, cost-effective, and high-quality analytical services. Underpinned by technology know-how and access to high-quality talent across the US, Europe, and Asia, we help our global portfolio of biopharmaceutical and CRO clients increase productivity and accelerate development, with robust data standardization and faster statistical reporting.
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.
ancillarie is a support service company established in 2012. Company provides support services in clinical research for Pharmaceutical, Biotechnology and Contract Research Organizations and helps them to accomplish their goal.
Aptus Clinical is a specialist UK-based Clinical Contract Research Organisation (CRO) with particular expertise in oncology, rare diseases and advanced, cell and gene therapies. We have decades of experience in delivering complex and innovative trials, transforming potential into value.
Bioforum is a data-focused contract research organization (CRO), serving clients worldwide in optimizing the collection, standardization, and reporting of clinical research data. We strive to consistently improve and innovate data processes, enabling the most efficient data submissions for our clients across the life sciences industry worldwide. From our offices in Israel, the U.S., Australia, and South Africa, our multidisciplinary team provides in-depth expertise and delivers high-quality solutions, including medical writing, data management, statistical programming and biostatistics.
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.
George Clinical is a leading global clinical research organization founded in Asia-Pacific headquartered in Sydney, Australia, driven by scientific expertise and operational excellence. With over 20 years of experience and more than 400 people managing 39 geographical locations throughout the Asia-Pacific region, USA, and Europe, George Clinical provides the full range of clinical trial services to biopharmaceutical, medical device, and diagnostic customers, for all trial phases, registration and post-marketing trials. George Clinical combines scientific and clinical leadership with expert trial delivery to create distinctive world-class solutions.
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.
Insights Research Organization & Solutions (IROS) is the first UAE-based Contract Research Organization (CRO) specializing in healthcare research. From clinical trials across all therapeutic areas to integration of real-world data, we provide the highest international ethical and scientific standards in clinical trial management, as well as key insights that lead to innovative, life-changing treatments.
While the drug discovery process is complex and critical, the clinical testing and validation phase is equally crucial, requiring procurement of proper resources and efficiency for optimal outcomes. IROS, with its expertise in data research, project management, testing, and trials, enables pharmaceutical companies to develop new medicines and drugs in a cost-effective manner, which will allow them to enter new products to market more efficiently. Our facilities meet the highest standards and optimize results through professional, productive teams and groundbreaking technologies that support and add value to research from conception to commercialization at national and international levels.
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.
KCR is a clinical development solutions provider creating value for biotechnology and pharmaceutical organizations.
Founded in 1997, our expert teams support clients with full-service clinical development capabilities across four main areas: Trial Execution, Consulting, and Placement .
KCR operates across North America, Europe, and Australia, with main office locations in Boston, US; Berlin, Germany; and Warsaw, Poland. Our geographical coverage across 25+ countries, cutting-edge technical capabilities and tailored offerings allow for the optimized delivery of solutions to develop life-changing therapies.
KCR offers access to an estimated population of 1.1 billion people.
Medical Agency for Research and Statistics is a clinical research consultancy and training corporate. #MARS provides several services for clients in the Clinical, bioequivelance, biotechnology and medical device sectors، both academic and regulatory:
Medical writing
Clinical data management
Biostatistics
Training courses
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
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.
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.
PPD is a Leading Global Contract Research Organization Focused on Delivering Life-Changing Therapies
As a global provider of clinical development and laboratory services, focused on operational excellence, we improve health by helping customers deliver life-changing medicines. Patients are always at the heart of our work. This is what drives us to continually reimagine – and reformulate – the future of pharmaceutical product development. We deploy our passion, innovative spirit and an exceptional span and quality of solutions to demonstrate the effectiveness, safety and value of new therapies.
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.
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.
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.
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