REGULATORY REQUIREMENTS AND REGULATORY OPERATIONS IN PHARMACEUTICALS
Saurabh D. Bhandare*
Abstract
Regulatory Agencies or Drug Regulatory Agencies in a pharmaceutical
industry acts as the operational interface between the pharmaceutical
companies and drug regulatory agencies or authorities that are to be
workforce for regulatory purpose across the world. These agencies
look after the regulatory requirement and setup standards and
procedural requirements for pharmaceutical products and API
manufacturing. These agencies are involved in regulatory operations
based on standard procedures which have specific operation procedures
called as SOP‟s that are known as Standard Operating Procedures. The
regulatory agencies sets standards based on clinical requirements and
obtained data for safety of drug and drug products as a pharmaceutical
product/API. The important roles of such agencies and authorities are based on evaluation of
clinical safety data and to ensure protection of human health ensuring all the parameter such
as: safety, efficacy and quality of drugs ensuring appropriateness and accuracy of products
information.
Keywords: Regulatory Agencies, U.S. FDA. MHRA.
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