Mr Jayant Kumar, delivered a talk on the topic “Regulatory Expectations for Quality Compliance - Proposed Revision of Schedule M”. He briefed about the importance of GMP in Pharmaceutical Manufacturing process. He explained about the background of GMP including about the role of drugs in Public Healthcare system, Import, Manufacture, Sale and Distribution of Drugs, Cosmetics and Medical Devices & Drug Regulations to ensure Safety, Efficacy and Quality etc. His talk continued with objectives and insights to manufacturers about Revised GMP and to aware about new provisions in the revised Schedule M, disseminate new provisions to all stakeholders well in advance and to make manufacturers ready for implementation.