New York, NY (PressExposure) February 25, 2013 -- Synowledge, a market leader known for its global and progressive approach to providing drug safety, regulatory affairs and related IT solutions to life sciences organizations, is pleased to announce the launch of its free Synowledge Webinar Series encompassing relevant industry topics in pharmacovigilance, regulatory affairs, and IT.
December 2012 marked the start of the newly revamped and comprehensive Synowledge Webinar Series, with a Regulatory Affairs webinar covering the Benefits and Risks of Outsourcing Regulatory Affairs. Synowledge hosted a webinar discussion on the Benefits and Risks of Outsourcing Medical Information Contact Centers earlier this month, with industry insights from an expert in Medical Information, Dr. Ajay Paghdal, Pharm.D.
Synowledge's latest Regulatory Affairs webinar titled "Applying the Advantages of the 505(b)2 Pathway" was hosted on Tuesday, February 19th, 2013. Other upcoming topics in Synowledge's webinar series include Aggregate Reporting, Medical Information Call Center Services, CSR Development: Industry Best Practices, and many others.
To attend or learn more about our Webinar Series, please visit http://www.synowledge.com/pv-services-news-events-webinars.html and register. Please contact email@example.com if you would like to arrange a personal webinar presentation on previous industry topics.
Synowledge welcomes feedback and suggestions on life sciences and IT related topics for future webinars in our dynamic series.
ounded 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.