GMP-Risikoanalysen (Original PDF from Publisher)

Risk analyzes are methods of quality risk management and play an important role. The pharmaceutical process comprises various areas, including product development, the compliant operation of production facilities, the procurement of raw materials, the production of product batches, testing in quality control, monitoring compliance with all regulations by quality assurance, documentation and the evaluation of abnormalities or deviations up to the storage and distribution of the products. Risk assessments are an essential tool that is applied to all of these levels and areas. The aim is to identify and evaluate risks in order to keep the risk sufficiently under control by means of suitable measures and thus to ensure product quality.

Product Details

• Publisher: Springer Fachmedien Wiesbaden; September 3, 2021
• Language: German
• ISBN: 978-3658352073
• ISBN: 9783658352073
• eText ISBN: 9783658352080