[b]New York, NY, August 20, 2013[/b] - Synowledge LLC, a premier IT Services company with strong domain and technical expertise in implementing and managing enterprise applications for life science organizations, is hosting a webinar to focus on industry perspectives of adoption of a CSV Hybrid model and how it will help companies to be in a audit-ready state. The free webinar will help key decision makers in IT Planning and Quality Assurance to identify strategies to address the key challenges and maximize effectiveness of employing a hybrid model.

"Consistent quality assurance and regular compliance maintenance initiatives in today's environment can only be attained by strategic implementation of a holistically driven Compliance Management Program. With the increasing operational and strategic usage of IT assets in driving core business process, it is imperative for regulated companies to balance the cost of quality with the cost of IT investments" said Somodipto Basu - Director - IT Services.

Sanjit Pal, our SME on Validation Services and Compliance Consulting is the main speaker for the CSV Hybrid Model webinar at 11:00 AM EST (4:00 PM GMT) on August 22nd 2013.

[b]About Synowledge[/b]

Synowledge is a global provider of Drug Safety, Regulatory Affairs, Biometrics, Clinical, and IT related solutions 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. With more than 20 years of industry experience, our core team members have worked with leading pharmaceutical, biotech, medical device, and health care provider organizations. Synowledge is headquartered in Stamford, CT, USA with operation facilities in 7 locations across Europe, North America, South America, and India. For more information, please visit [url=www.synowledge.com]www.synowledge.com[/url].