How to Maintain Data Integrity in Pharma Cloud Systems | ALCOA+ & Compliance Guide (2025) скачать в хорошем качестве

How to Maintain Data Integrity in Pharma Cloud Systems | ALCOA+ & Compliance Guide (2025)

How to Maintain Data Integrity in Pharma Cloud Systems | ALCOA+ & Compliance Guide (2025) Switching to cloud systems in pharma? Learn how to maintain data integrity and meet GxP compliance with ALCOA+ principles, validation, and vendor oversight. This guide will help you stay audit-ready in 2025.” In this video, we cover everything you need to know about data integrity when moving to cloud systems in the pharmaceutical industry. Cloud adoption is accelerating in pharma, but regulators like the FDA, EMA, and MHRA expect strict adherence to ALCOA+ principles and data integrity best practices. You’ll learn: ✔️ What regulators expect (FDA, EMA, GxP) ✔️ Common risks during cloud migration ✔️ How to apply ALCOA+ in cloud environments ✔️ Validation, audit trails, and vendor management tips ✔️ Best practices for maintaining compliance If you’re implementing cloud-based QMS, LIMS, or eBatch Records, this video will give you a clear roadmap to protect your data and stay compliant. 👉 Subscribe to Pharmalytics for more insights on GMP, quality, and pharma regulatory updates. #Pharma #DataIntegrity #GMP #CloudSystems #PharmaCompliance #Pharma #DataIntegrity #GxP