In order to adapt to the new situation and development of China's pharmaceutical industry and improve the quality of drugs through stricter and more comprehensive drug production quality management standards, the Ministry of Health implemented the 2010 revised version of GMP from March 1, 2011. According to the new version of GMP requirements, GMP certification has changed from static to dynamic, which means that the requirements for clean rooms are becoming increasingly high. Pharmaceutical companies need to carry out comprehensive quality control from design, construction, and later operation management to meet the requirements of the new GMP. As an important stage in the formation of a clean room, construction requires construction personnel to strictly follow the requirements of the clean room for production and installation. The clean air conditioning system, purified color steel plate system, and clean floor are important components of the clean room, ensuring high-quality and high-level construction to ensure the smooth passing of GMP certification.
1. Preparation work
Before installing the inner corner of the purification board arc, the following tools and materials need to be prepared: woodworking saw, electric drill, wrench, screwdriver, waxed cardboard, purification board, clip, glue, etc.
2. Installation steps
Suzhou Pharma Machinery Co.,Ltd.
2024/09/27
Gino