Affiliations

ARM-logo-sm The Alliance for Regenerative Medicine (ARM) is the preeminent global advocate for regenerative and advanced therapies. ARM fosters research, development, investment and commercialization of transformational treatments and cures for patients worldwide. Learn more about the ARM at alliancerm.org

acrp-prcPRC Clinical is proud to be an active sponsor and supporter of ACRP. The association 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. In 2016, PRC Clinical received the Annual Sponsor Award from the ACRP Northern California Chapter.

PRC Clinical is a member of the California Life Sciences Association (CLSA), the leading voice for California’s life sciences sector. CLSA works closely with industry, government, academia and other stakeholders to shape public policy, drive business solutions and grow California’s life sciences innovation ecosystem. CLSA serves over 750 biotechnology, pharmaceutical, medical device, and diagnostics companies, research universities and institutes, investors and service providers. CLSA was founded in 2015 when the Bay Area Bioscience Association (BayBio) and the California Healthcare Institute (CHI) merged to create the state’s most influential life sciences advocacy and business leadership organization.

 

Strategic Alliances

 

Veeva Vault is a true cloud enterprise content management platform and suite of applications specifically built for life sciences. Traditionally, companies have had to deploy applications for content and separate applications to manage associated data. Veeva Vault is the only content management platform with the unique capability to manage both content and data. Companies can now eliminate system, site, and country silos and streamline their end-to-end clinical processes. Because all Vault applications are built on the same core platform, companies gain additional efficiency and compliance through the streamlined flow of documents across regions and departments. Content stays accessible, current, and in context across the entire development and commercial lifecycle. Visit www.veeva.com.

The pioneer of independent ethical review, WCG continues to drive ingenuity in the clinical research space. Today, WCG’s solutions are built upon the foundation of ethical review, but have grown to include a suite of complementary services and technologies that expand the capabilities of the modern research professional. WCG delivers transformational solutions that stimulate growth, foster compliance, and maximize efficiency for those who perform clinical trials. WCG is proud to serve the individuals on the frontlines of science and medicine, and the organizations that strive to develop new products and therapies to improve the quality of human health. It is our role to empower them to accelerate advancement, while ensuring that the risks of progress never outweigh the value of human life. Visit www.wcgclinical.com.

SDC SDC is committed to providing experienced teams who will take ownership of your needs and are positively engaged in your projects. SDC delivers leading-edge statistical analysis and data management services to pharmaceutical, biotechnology, and medical device companies, as well as CRO partners. With biostatistics, clinical data management/EDC, and interactive response technology (IRT) expertise at our core, SDC also provides scalable full service clinical trial solutions via our diverse and complementary strategic partnerships. Speak with us today about how SDC will take ownership of your clinical project needs. For more information, please visit www.sdcclinical.com, call 480-632-5468, or email data@sdcclinical.com.

Cenetron-Central-Laboratories Cenetron is an industry leading central laboratory, supporting global companies in Phase I to Phase IV clinical trials. Cenetron offers complete central laboratory services, including protocol review, technology consultation, laboratory testing, and clinical study data management. Cenetron occupies 43,000 square feet of newly constructed administrative, clinical and research laboratory space, as well sample storage and kit manufacturing facilities. Cenetron also offers custom assay development and companion diagnostic tests, which are developed to provide Pharma clients with the latest tools for screening, randomizing, and monitoring patients.