Safety and quality management in drug production areas

In the pharmaceutical industry, maintaining high-quality air levels is crucial for the quality of drugs. Therefore, it is necessary to strictly follow relevant regulations and standards to monitor the processing, packaging, and storage areas of drugs.

The proper storage of drugs is crucial to people's health, therefore, continuous pressure and temperature monitoring should be carried out in various areas of pharmaceutical factories.

Solman recently provided 70 units to IBSA Pharma Inc in CaliforniaCP210 series multifunctional transmitterUsed to build the company's pharmaceutical production line, including laminar flow chambers (LAFs).

The CP210 series multifunctional differential pressure temperature transmitter includes multiple models of products, which can be used to continuously monitor environmental differential pressure, temperature and other parameters. Paired with Debimo airfoil multi-point average wind speed and air volume measuring blades, it can also monitor environmental wind speed and air volume. combineHigh precision, high cost-effectivenessThe advantages.

Overall design requirements for clean rooms

The design of clean room facilities in the pharmaceutical industry should not only meet the relevant regulations of GMP, but also comply with relevant national laws and regulations, implement current standards and specifications, meet practical, safe, and economic requirements, save energy and protect the environment.Actively adopt advanced technologies whenever possible, to meet current production needs while also considering future development.

The inner surface of the clean area (walls, floors, ceilings) should be smooth, without cracks, tightly connected, and free of particle shedding, avoiding dust accumulation and facilitating effective cleaning. If necessary, disinfection should be carried out.