SAN BRUNO, Calif.--(BUSINESS WIRE)-- PRC Clinical®, a privately held Contract Research Organization (CRO) providing clinical research management services announced today that it has joined BayBio, Northern California’s life science association promoting the regional life science community through advocacy, enterprise support, and enhancement of research collaboration.
“We are committed to the spirit of the non-profit and advocacy work of BayBio and are delighted to join forces with other local companies engaged in life-saving and leading-edge research,” said PRC Clinical Co-Founder and Chief Operations Officer, Tony Taricco. “PRC Clinical is pleased to be a member of such a well-respected and professional organization, and we look forward to providing our CRO services to sponsors companies and other partner members of the group.”
BayBio is an independent, non-profit 501(c)(6) trade association serving the life science industry in Northern California. The staff and services of BayBio are paid primarily through memberships, sponsorships, and event registration fees. BayBio provides these services through representatives in South San Francisco and through coalition partners in Washington, DC. Follow us at twitter.com/baybio and like us on Facebook at facebook.com/baybio.
About PRC Clinical
PRC Clinical™ is a privately held Contract Research Organization (CRO) in the San Francisco Bay Area, offering Phase I-IV clinical trial management services for virtual, small and mid-size pharmaceutical, biotechnology and medical device companies. PRC Clinical has forged strategic alliances with key preferred providers to offer a full suite of CRO services and provide our clients with quality, innovation, and rapid study start-up and execution, from proof-of-concept through regulatory approval.
PRC Clinical project teams are comprised of highly skilled and experienced clinical professionals. Our services include Project Management, Regional Monitoring, Data Management, Electronic Data Capture (EDC), Biostatistics, Medical Monitoring, Regulatory Consulting, Pharmacovigilance, Interactive Web Response System (IWRS), Quality Assurance/Audits, Central Laboratory Services and Clinical Payment Services. PRC Clinical has experience in conducting Phase I-IV trials, including Registries and Orphan Drug studies, as well as a broad range of experience in the many therapeutic areas. For more information, please visit www.prcclinical.com
Saira Singh, 877-519-6001
Source: PRC Clinical