It is the standard that defines the conditions to be applied during the establishment of Quality Management Systems and is subject to certification audit. Is the name of the issued document.
Affiliated to the Ministry of Health of the United States of America; It is an office responsible for dietary supplements, food, medicine, blood products, biological medical products, radiation-emitting devices, medical devices, veterinary instruments and cosmetics.
Good manufacturing practices are a quality system that guides manufacturers in what and under what conditions the products such as food, pharmaceuticals, cosmetics and medical devices that can affect human health, especially in many sectors in our lives, should be produced in accordance with the GMP standard.
A certificate type is determined for each product that is “suitable” in terms of Islamic criteria and humanitarian requirements, and it is aimed to meet both the producer and the consumer on a common ground.