2023年6月9日 4 分钟
EudraLex Volume 4 Annex 11: compliance checklist and future prospects
This article addresses the latest revision of EudraLex Volume 4 Annex 11 and provides a checklist for compliance. Download it now.
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Qualification & Validation2022年11月15日 6 分钟
Annual Product Quality Review (APQR / PQR) in Pharma: importance, benefits & challenges
Learn more about the importance, benefits, and key challenges related to Annual Product Quality Review in Pharma (APQR/PQR).
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Software Solutions & Services2022年10月6日 4 分钟
21 CFR Part 11 compliance checklist: does your system comply?
21 CFR Part 11 regulates the use of electronic records and signatures in pharma and MD. Download our 21 CFR Part 11 compliance checklist here.
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Software Solutions & Services2022年5月3日 2 分钟
Data migration in CSV: definition, purpose, and best practices
Sometimes it is necessary to perform data migration in computer systems, applications, or software. Learn more about the importance and risks.
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Software Solutions & Services2022年4月5日 4 分钟
What is decommissioning in CSV?
In CSV, decommissioning is the retirement or controlled shutdown of a computer system that is no longer needed. Learn more about this process.
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Software Solutions & Services2021年4月26日 5 分钟
10 things you should know before validating Computerized Systems
The steps you need to follow when you want to start validating a computerized system. Check these 10 steps!
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