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Regulatory departments are continually being asked to do more with less. In addition, regulatory authorities are increasing the
scrutiny related to patient safety and compliance. As regulatory departments are challenged to develop both domestic and
global regulatory strategies, coupled with the corporate desire to launch in products in the markets early, the need to understand
the regulatory requirements for filing, timelines, what products are approved in which markets is becoming a critical regulatory
need for both industry and regulators. Effective regulatory information management processes with appropriate tools are needed
to ensure the organization remains compliant with its product registrations.
"Bobby George is currently the Assistant Vice President & Head of Regulatory Affairs at Reliance Life Sciences, Navi Mumbai. He has done his M.
Pharm and Ph.D. in Pharmacology from Panjab University, Chandigarh. He has over 14 years of industrial experience. He is the recipient of several
national awards and has published more than 24 papers in reputed journals. He is also an editorial board member for two of the journals?.
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