The quality assurance of drugs is the core of the development of the pharmaceutical industry, and the impact on the quality of drugs comes from many aspects, among which the production environment, production conditions and production equipment are the most important aspects. In pharmaceutical production, contamination from the environment and production conditions includes bacteria, dust, operational errors and cross-infection. The main thing involved in pharmaceutical equipment is the lack of effective pollution prevention and control measures. The quality of drugs is related to thousands of households. Every link in the pharmaceutical process must be strictly controlled. It is necessary for pharmaceutical equipment to fully implement the elimination of pollution sources from various situations outside drug production. The elimination of sources of contamination from various situations outside of drug production is something that pharmaceutical equipment needs to adequately perform.
In recent years, drug quality and safety problems caused by drug contamination caused by the pharmaceutical profession's failure to pay attention to anti-pollution measures in the production process have been frequently reported. To produce drugs that meet the quality requirements, pharmaceuticals must have qualified staff and hardware and software facilities that meet the industry's GMP standards.
Pharmaceutical equipment involves pharmacy, pharmaceutical technology, biotechnology, chemistry, metal materials, mechanical principles, electrical engineering, refrigeration technology, HVAC technology, hydraulic and pneumatic technology, computer and other applied disciplines, with extremely complex characteristics. With the rapid development of science and technology and the pharmaceutical industry, pharmaceutical equipment plays an increasingly important role in the field of medicine, which can effectively improve the technical content of drugs, promote the automation, information and intelligence of the production process, ensure the standardization of product quality, and promote the intensive development of the pharmaceutical industry.
First of all, in the design and manufacture of pharmaceutical equipment, it should meet the requirements of drug production and technology, safe, stable, reliable, easy to clean, disinfect or sterilize, facilitate production operation and maintenance, and prevent errors and cross-contamination. Pay attention to the selection of non-toxic, non-radiation, more stable materials and their ability to adapt to the special environment of drug production.
Secondly, the most important point is the prevention and control means of pharmaceutical equipment for pollution in production. The pharmaceutical process is complicated, which also determines the multi-function of pharmaceutical equipment, meets the requirements of use, conforms to GMP and effectively carries out pollution prevention and control, reduces drug pollution in the production process, and achieves the purpose of ensuring the quality requirements of drugs. Pollution prevention and control can be carried out in terms of function, appearance structure, material selection and equipment verification.
Pharmaceutical equipment is the protective wall of drug safety, so the design and manufacture of pharmaceutical equipment need to meet the requirements of relevant industry standards, reduce pollution factors, and have a good prevention and control of pollution. (Source Internet)
