Company Name: Hangzhou Qiaohui Color Steel Co., Ltd. <br> Contact: Mr. Du <br> Contact: 15068169318
Address: No. 18 Dongjiamen, Sandun Town, Xihu District, Hangzhou
In the early 1980s, China formally introduced the concept of GMP, the "Good Manufacturing Practice for Drugs." What is GMP?
GMP is a standard that must be observed when designing a GMP clean room, and it is also a lower standard that the GMP workshop design must adhere to. The content stipulated by GMP is a relatively basic condition that pharmaceutical processing enterprises must meet. Therefore, for the biopharmaceutical industry, the construction of GMP clean rooms is the first prerequisite and mandatory specification for all work. Today, I will explain in detail the construction and design standards of GMP purification workshops / GMP laboratories.
Dust-free purification workshop
I. Connotation of GMP standard
In brief, GMP requires that production enterprises should have good production equipment, reasonable production processes, perfect quality management and strict testing systems to ensure that the quality of subsequent products (including food safety and hygiene) meets regulatory requirements. Enterprises need to form a set of operable operating standards in terms of raw materials, personnel, facilities and equipment, production processes, packaging and transportation, and quality control to improve the sanitary environment of the enterprise.