Synowledge specializes in providing drug safety and pharmacovigilance services to small, mid and large sized pharmaceutical and biotechnology companies. Our team consists of highly qualified and skilled experts who are committed to helping life sciences companies meet the challenging demand of producing detailed and accurate safety reports within the regulatory timelines. Synowledge’s broad range of solutions include full case management (incl. case intake, data entry, coding, triaging, QC, medical review, submission, etc.), generation of expedited and periodic reports, Qualified Person for Pharmacovigilance (QPPV) services, medical literature review, analysis and trending of cases (signal detection), and call center services that handle medical inquiries/information, AE/SAE case intake and product complaints.
Additionally, Synowledge provides related IT services to help life sciences companies manage and maintain their drug safety and other critical applications. With a global presence, and market-leading technologies, Synowledge ensures reliable and high performance solutions.