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
4Pharma is a Scandinavian contract research organization (CRO) providing medical research services to pharmaceutical, biotechnology, medical device and food companies.
Focused on biostatistics, data management and medical writing, 4Pharma employees offer you a unique blend of industry experience, service provider flexibility and the academic excellence of truly data driven mindsets.
Our core focus lies on customer satisfaction and quality of work.
With the experience of several successful global regulatory submissions, hundreds of studies we conducted for our clients (or accompanied with scientific advice) and finally our open minded dedication to science – we, the people at 4Pharma are dedicated to take you
We are not a fruit shop, but we do help our clients sort out their apples from their oranges! Established in 2018, A&O was set up as a niche Contract Service Organisation, offering custom-built reporting tools for clinical operations, data management and medical departments.
We provide off-the-shelf solutions that harness existing standard MS Office installations, requiring no additional software, that can be utilised in any clinical data environment. This approach is born out of years of knowing the ‘customer’; DMs, CTMs, Operations, CRAs, study physicians who do not want to work with heavy data listings or overly complex systems. They want a no nonsense, interactive solution in an MS Office environment that they understand. As our solutions reside outside of clinical management systems such as EDC, CTMS or external lab data, A&O can typically bridge the gap between these systems and their differing data formats (e.g. “I can see in the EDC that this patient had samples taken at visit 4, but have no idea where these samples are now”). From customised tooling to help with clinical study oversight, visit forecasting, data reconciliation (e.g. IWRS vs EDC, lab data…), medical review reports to data metrics/KPIs, A&O can assist in creating an effective solution.
If you are drowning in data and require a tailored tool to help you manage or review it, please get in touch: www.apples-and-oranges.co.uk
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.
Bionical Emas is the only CRO to combine Clinical Development, Early Access Programs and Clinical Trial Supply, to deliver a unique, seamless approach supporting our clients to bring new medicines to patients faster.
Business & Decision Life Sciences is a specialized high-tech CRO and Resourcing company, taking advantage of digital technologies to optimize collection, transformation and usage of Life Sciences Data by adapting to new industry evolution and regulations.
Cmed is an innovative, full-service, technology-led CRO, established in 2000 by a team of experts passionate about helping customers deliver highly successful clinical trials. We bring together an experienced team and our own innovative technology to inspire and drive real progress throughout the clinical trial process – for every step, every solution, every study. encapsia®, our new generation Clinical Data Suite is just one example of our realization of this ambition, devising new ways to drive complex clinical trials and achieve greater, speedier and more accurate results. Our vision is to conduct clinical trials better than any other CRO to help patients and ultimately save lives.
We have earned a strong reputation for successfully delivering complex, demanding and innovative clinical trials in various therapeutic areas, with considerable therapeutic expertise in both oncology and rare disease
As the drug development business of Laboratory Corporation of America Holdings (LabCorp) and the world’s most comprehensive drug development service company, we have helped pharmaceutical and biotech companies develop 100% of the top 50 prescription drugs in the marketplace today.
Because of our broad experience and specialized expertise, we’re in a unique position to supply insights that go above and beyond testing. Together with our clients, we create solutions that transform potential into reality
CROS NT is a data-driven Contract Research Organization (CRO) providing services from feasibility to clinical study reporting for Phases I-IV and medical device trials.
CROS NT’s services include regulatory consultancy, monitoring, data management, biostatistics programming & analysis, pharmacovigilance and medical writing – and accompanying eClinical applications (data visualization, EDC, IWRS, eCOA/ePRO etc.). All services are underpinned by strong clinical and biometrics project management.
We offer a center of clinical and data excellence by facilitating data visualization, risk-based monitoring, regulatory submissions, data standardization and traceability to improve efficiency and substantially reduce costs.
CROS NT works with a wide portfolio of Sponsors – from large pharmaceutical companies to small and mid-size pharma, biotech and medical device companies – to define the best outsourcing strategy: whether that be a full service, centralized biometrics approach, Functional Service Provision or case-by-case consultancy
CROS NT is a data-driven Contract Research Organization (CRO) providing services from feasibility to clinical study reporting for Phases I-IV and medical device trials.
CROS NT’s services include regulatory consultancy, monitoring, data management, biostatistics programming & analysis, pharmacovigilance and medical writing – and accompanying eClinical applications (data visualization, EDC, IWRS, eCOA/ePRO etc.). All services are underpinned by strong clinical and biometrics project management.
We offer a center of clinical and data excellence by facilitating data visualization, risk-based monitoring, regulatory submissions, data standardization and traceability to improve efficiency and substantially reduce costs.
CROS NT works with a wide portfolio of Sponsors – from large pharmaceutical companies to small and mid-size pharma, biotech and medical device companies – to define the best outsourcing strategy: whether that be a full service, centralized biometrics approach, Functional Service Provision or case-by-case consultancy
DataClin was established in 2010 as the first Contract Research Organization (CRO) in the MENA region specialized in clinical data management, biostatistics and medical writing.
DataClin grew to be one of the top leading CROs in the MENA region working according to a full set of standards covering our scope of work, with an ongoing process of updates with regulatory requirements, and compliance to the international standards, guidelines and customer specific standards.
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.
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
We provide the pharmaceutical industry with an alternative approach to clinical trial design and management. We help you safely accelerate drug development programs, thereby enabling critical new drugs to reach patients faster. We are the leading experts in the field of electronic health records (EHRs) enabled randomised clinical trials (RCTs). We provided the technology that enabled the success of the Salford Lung study and are the only organisation in the world to have evaluated the safety and effectiveness of a pre-license medicine in a real-world setting
The Oncology Clinical Trials Office (OCTO) works with investigators to deliver trials in medical oncology, radiotherapy and imaging from the first-in-human drug trials to large clinical studies across a range of tumour types.
We have particular expertise in delivering early phase multi-centre trials for biologically distinct populations
OCTO is the oncology division of the UKCRC registered Oxford Clinical Trials Unit (OCTRU) and a member of the NCRI Cancer CTUs Working Group
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.
With a global headcount of in excess of 1,500 employees across 31 countries, Premier Research continues to enjoy growth and expansion.
Premier Research is not about being everything to everyone. Instead, our deep, focused expertise targets the therapeutic areas and indications where today’s biotech and specialty pharma pioneers are doing the most amazing work. We’re over 1,500 employees strong and operate in more than 20 countries, delivering unmatched expertise, operational skills, and dedication to meeting customers’ most challenging needs.
Interested to join us and meet some of the brightest minds in clinical development today — people who apply their best to every project, recognizing that what they do significantly affects the lives and well-being of customers, patients, physicians, and colleagues? If so, please feel free to visit the careers pages of our website to apply for current openings https://premier-research.com/careers/
You’ll enjoy great benefits and very flexible working conditions in a company which values your contributions, rewards your achievements, and is committed to helping you reach your full potential.
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.
TFS was founded in 1996 and has grown to become the leading global mid-size clinical CRO focusing on small and mid-size life science customers. TFS employs more than 700 professionals throughout 21 countries and currently delivers clinical research services in more than 40 countries. We can provide end-to-end solutions or flexible single services. Our partnering approach with customers is based on our four business principles – commitment, flexibility, value creation and global reach. Our core therapeutic specialties are Dermatology, Oncology, Ophthalmology, Immunology, CNS, Cardiovascular and Endocrinology.
Worldwide Clinical Trials employs more than 1,400 professionals around the world, with offices in North and South America, Eastern and Western Europe, Russia and Asia. One of the world’s leading, full-service contract research organizations (CROs), we partner with sponsors in the pharmaceutical and biotechnology industries to deliver fully integrated clinical development and bioanalytical services, extending from first-in-human through phase IV studies
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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