Regulatory Affairs (RA) play critical roles in a pharmaceutical industry as it concern about the product lifecycle, it provide strategic and operational direction and support for working within regulations to expedite the development and delivery of safe and effective products to our patients. We develop and execute a regulatory strategy to ensure that the efforts of the drug development team results in a product that is approvable by global regulators and also to ensure that the company's activities, from non-clinical research, production, testing to advertising and promotion are conducted in accordance with the regulations and guidelines established by regulatory authorities. Here at Memphis Vision Care Pvt. Ltd., We strictly adheres to cGMP (Current Good Manufacturing Practices) and Schedule M that results in products compatible in every regulatory market across the world.