GMPC/FAD QSR820 Medical Management System

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1. Introduction to GMPC/FAD QSR820
In 1992, the FDA issued the Cosmetics GMP Guidelines to guide cosmetic manufacturers to regulate the production of their cosmetics to ensure the hygiene and safety of cosmetics. In order to ensure that cosmetics produced and sold in its territory (including imported from outside the EU) do not harm consumers' health, the European Union issued the Cosmetics Directive 76/768/EE on July 26, 1976, in February 2003. The latest directive (seventh edition) was issued on the 27th. The latest directive requires factories that produce cosmetics to meet good operating practices, with a focus on ensuring the safety and hygiene of the cosmetic process and preventing foreign matter, poisons, and microbes from contaminating the product.
Cosmetics sold in the US and EU markets must comply with the US Federal Cosmetics Regulations or the EU Cosmetics Directive----GMPC is called Guideline for Good Manufacture Practice of Cosmetic Products, and Chinese is called Good Manufacturing Practices to ensure the normal use of consumers. After the health.

2. Benefits of GMPC:

1. Ensure product safety;
2. Improve product quality;
3. Eliminate dangerous accidents;
4. Reduce the risk of injury or death caused by the product to the consumer;
5. Reduce the risk of product recycling;
6. Compliance with regulations and trade guidelines;
7. A good working environment;
8. Effective cost control and international recognition;
9. Enhance product competitiveness;
10 effective product traceability.

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