This webinar is intended to help you get familiar with FDA’s Quality System Regulations (cGMP) for medical devices. GMP covers all aspects of production from the starting materials, premises, and equipment to the training and personal hygiene of staff. Detailed written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process – every time a product is made. This webinar will introduce you to the importance of GMP and the basic requirements you must comply with.
