The latest in the field of Pharma
Dear reader,
Staying ahead in the pharma industry means keeping up with evolving regulations, best practices, and innovative solutions.
In this edition, we bring you must-read insights on software validation, GMP facility qualification, pharmacovigilance, sterilization validation, and more. Plus, don’t miss our top downloads and upcoming events.
Let’s dive in. Happy reading!?
Antonio Borregon?| Head of Pharma BD Global
TOP DOWNLOADS
GAMP 5 Software Validation Approach for GMP, GCP and GLP regulations
This whitepaper will first give you insights into which?guidelines?are applicable, in which setting, and how to comply with these guidelines. A comparison will be made between the different fields and how?GAMP5?can be used to comply with each of these regulatory frameworks.
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New GMP Facility Qualification: set-up, process and best practices
In this white paper, we delve into the complexities of establishing a new GMP facility. We focus on potential pitfalls and best practices to provide a comprehensive overview.
How to import your products into the EU
Are you a medicinal product manufacturer looking to import your products into the EU in line with the latest EU-GMP import regulations? Be sure to download our free EU GMP guide!
领英推荐
OUR MUST-READS
SEE YOU AT THIS EVENT?
May 7-8 ?? | Antwerp, Belgium ??
We are attending flanders.bio’s annual Knowledge for Growth business conference, attracting decision makers from biotech, pharma and medtech, agricultural and chemical industries as well as investors, universities, topnotch research institutes, policymakers and competence providers. See you there?
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Qual & Val Engineer at QbD | Pharma & Biotech
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