Founded in 2006, Synowledge specializes in providing drug safety, regulatory affairs and related IT services to small, mid, and large sized pharmaceutical, biotechnology and medical device companies. Our comprehensive outsourcing solutions combine the unique strengths of both onshore and offshore services to meet our clients’ needs. Synowledge is headquartered in Stamford, CT, USA with operation facilities located in Ohio, the United Kingdom, Germany and Bangalore, India. Synowledge’s broad range of solutions and KPO services 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 a call center services that handles medical inquiries/information, AE/SAE case intake and product complaints.
Synowledge also provides IT services to help life sciences companies manage and maintain their drug safety applications as well as other critical applications . With a significant global presence, and market-leading technologies, Synowledge ensures reliable and high performance solutions.