What is the role of temperature and humidity verification in the pharmaceutical industry?

In the GMP implementation process, special emphasis on process and equipment validation, through the validation, can ensure that the entire production process in the expected controllable range of normal operation, colleagues can be optimized for the production process of a variety of parameters, to greatly reduce production costs, temperature validation system is to meet the new GMP requirements for pharmaceutical, biotechnology and medical device production and the crash of the door to the design of a new type of Validation system. In short, validation is the government standardization requirements, product quality assurance, but also a way to reduce costs and risks. Shandong Huaxiang verification SINSE is committed to temperature and humidity verification.