GMP detailed actual QA workflow

First of all, first carefully read the requirements of GMP to understand what GMP needs to do, whether it is validation ah, or a variety of documents, or staff skills, equipment requirements, etc. Understanding and then according to the requirements of GMP to document the supplemental documents first, and then from the system above to establish a sound GMP is the meaning of good operation QA is a quality risk control, so it should be from the various factors that can affect the equipment to start so as to better comply with the requirements of GMP. QA is a kind of quality risk control, so it should start from the various factors that can affect the equipment so as to better meet the requirements of GMP QA quality risk control is mainly reflected in the IQC PQC OQC three major items, namely, incoming inspection, product production process inspection, product shipment quality inspection, etc. QA in fact, what we have to do is to do from the entire product production process and process to do some of the product quality can affect the quality of the product some of the validation of the food, pharmaceutical, or medical device industry, such as purified water, sterilized water and so on, all need to do. Purified water, sterilization, etc. are required to have the appropriate verification of the specific work or need to do their own according to the actual situation of the plant and the requirements of the GMP I hope you can see after the give a praise