Weighing Subject to the Requirements of “Good Manufacturing Practices”
22 November 2016
Pharmaceutical production and testing must be carried out under the regulatory requirements of “Good Manufacturing Practices” (GMP) and “Good Laboratory Practices” (GLP). This whitepaper describes the MSA125P-100-DI analytical balance from the Cubis® range and how it is suitable for pharmaceutical applications. The whitepaper details aspects of the design, qualification and cleanability and software and explains how these meet GMP regulations.