Translation of Pharmaceutical Engineering Terminology

Pharmaceutical engineering involves the design, development, and operation of processes and equipment used in the pharmaceutical industry. Here are some key terms and their translations:

Pharmaceutical engineering is the branch of engineering that focuses on the design and operation of processes and equipment used in the pharmaceutical industry.

GMP is a system for ensuring that products are consistently produced and controlled according to quality standards. It is essential in the pharmaceutical industry to ensure the safety and efficacy of drugs.

A cleanroom is a controlled environment where the concentration of airborne particles is minimized to ensure a sterile production environment.

HVAC systems are crucial in pharmaceutical facilities to maintain proper temperature, humidity, and air quality for the production of drugs.

Fermentation is a process used in the production of antibiotics and other pharmaceutical products where microorganisms are used to produce desired compounds.

Filtration is a separation process used to remove solid particles from liquids or gases in pharmaceutical manufacturing processes.

Validation is the process of establishing documented evidence that a system or process consistently produces results meeting predetermined specifications.

Sterilization is the process of killing or removing all forms of microbial life, including bacteria, viruses, and fungi, to ensure the sterility of pharmaceutical products.

A batch record is a document that provides a complete history of a batch of pharmaceutical product, including production, testing, and packaging information.

Process validation is the documented evidence that a process consistently produces a product meeting its predetermined specifications and quality attributes.

These are just a few key terms in pharmaceutical engineering. It is important to have a good understanding of these terms to work effectively in the pharmaceutical industry.