Commissioning and qualification are vital phases in the validation process of the pharmaceutical industry. Learn how these phases ensure quality and.
Why is it important to test glove integrity in isolators or rabs and when should it be done? What norms and regulations apply to glove integrity.
What is the purpose of the document about Commissioning and Qualification of a laboratory instruments, and how it can be implemented?
Do you know FAT and SAT? Learn their differences, and why they are essential for demonstrating equipment quality, compliance, and performance.
Are you aware on the importance of project management? Read to understand about quality compliance and the steps for a successful project completion.
Discover the complexities of the pharmaceutical product process, and the journey from raw material to final packaging.
Zoltan Langosco di Langosco, PQE Group's expert in Validation, explores the ASTM E2500 approach in all of its stages.
