Our Partners

SCDM Corporate Partners

Bioforum is a data-focused CRO providing a wide range of clinical data services to include medical writing, data management, clinical programming, biostatistics and pharmacovigilance.

Bioforum’s goal is to consistently improve and innovate data processes to support clients in the utilization of their clinical data and guarantee its integrity and accuracy for the most efficient data submissions.

With a multi-disciplinary team of experts, Bioforum provides unique and high-quality solutions for efficient collection, standardization and reporting of clinical research data.

Bioforum is a multinational company with offices in Israel, USA, Australia and South Africa.

Castor is the end-to-end data solution that enables researchers to easily capture, standardize, and integrate data from any source on one platform. These tools were created by researchers to ensure medical research data becomes reusable and machine-readable. Thousands of academic, medical device, and biotech researchers around the world are using Castor EDC, ePRO, and eTMF to efficiently conduct their studies and maximize the impact of their data. By making this technology accessible to anyone, Castor is helping researchers accelerate the discovery of treatments and cures.

Covance, a global contract research organization, worked on all of the top 50 best-selling drugs available today through its full spectrum of nonclinical, clinical and commercialization services.

Together with our clients, Covance transforms today’s healthcare challenges into tomorrow’s solutions.

For more than a century, MSD has been inventing for life, bringing forward medicines and vaccines for many of the world’s most challenging diseases. Today, MSD continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.

PAREXEL provides the most comprehensive drug development capabilities of any CRO worldwide.

Our purpose is grounded in our commitment to fund programs that provide public benefit, advance medical care and improve patient outcomes. Our belief is that all people deserve to live healthy lives. This drives our desire to provide access to medicines that are safe, effective, and affordable.

PRA Health Sciences delivers innovative drug development solutions that improve patients’ lives. Our people work tirelessly to provide quality results for clients. We offer specialized expertise across all phases and therapeutic areas and a broad spectrum of full-service and strategic solutions. With 16,000+ employees covering 90+ countries, we give you the global presence you expect, combined with an in-depth knowledge of local regulations, standards of care, and cultural customs.

Veeva Vault CDMS unifies best-of-breed applications for clinical data management including EDC, coding, cleaning, and reporting.

Vault CDMS is built on a modern cloud platform with a flexible and intuitive user interface. Vault EDC allows you to run complex multi-arm adaptive trials and make mid-study amendments without downtime or migrations. And a next generation interface for data monitoring and review helps CRAs work quickly and accurately and eliminates time spent paging through forms.

Together with Vault CTMS, Vault eTMF, and Vault Study Startup, Veeva Vault Clinical applications will help streamline clinical trials from study start-up to close.

SCDM Global Partners

The Association of Clinical Research Professionals (ACRP) supports clinical research professionals through membership, training and development, and certification. Founded in 1976, ACRP is a Washington, DC-based non-profit organization with more than 13,000 members who work in clinical research in more than 70 countries.
ACRP’s vision is that clinical research is performed ethically, responsibly, and professionally everywhere in the world. ACRP’s mission is to promote excellence in clinical research.

CDISC is a global, open, multidisciplinary, non-profit organization that has established standards to support the acquisition, exchange, submission and archive of clinical research data and metadata. The CDISC mission is to develop and support global, platform-independent data standards that enable information system interoperability to improve medical research and related areas of healthcare. CDISC standards are vendor-neutral, platform-independent and freely available via the CDISC website.

PharmaSUG is a Software Users Group of life science and health research professionals focused on the application of technological solutions in data analytics and regulatory support.

PharmaSUG’s premier event is our annual U.S conference. In addition, they hold an annual China conference as well as Single-Day Events throughout the year.

PharmaSUG is governed year round by an all-volunteer Executive Committee of past and future conference chairs, and a volunteer Conference Committee organizes each conference.

MCC —a trusted partner in the clinical trials industry — identifies what to measure and how to assess the critical components of what is changing and how the industry is responding to address the changes to make improvements. MCC continually brings you new insights into the leading trends within the industry.

Become a Corporate Partner

Corporate Partnerships

Corporate partnership with SCDM provides leading companies with significant, consistent and exclusive opportunities to gain access and exposure to a global network of clinical data managers and key opinion leaders.
We offer customisable partnerships you to help support your business objectives and meet your goals.
Download the brochure below for all the information on the SCDM Corporate Partner Program, and contact us to discuss how we can help to create the most valuable opportunities for your company.

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