CSV Training for Regulated Industries
Practical, regulation-ready training for pharmaceutical and life sciences professionals. Covering GAMP 5, 21 CFR Part 11, and EU Annex 11 — written and delivered by a working CSV consultant.
Everything you need to validate with confidence
GAMP 5 Aligned
All content follows current ISPE GAMP 5 guidance and reflects real-world regulatory expectations from the FDA and EMA.
Self-Paced Learning
Work through modules at your own pace with built-in progress tracking. Return to any module at any time.
Member Resource Library
Access a growing library of articles and Regulatory Watch summaries alongside your training, all included in membership.
One subscription. Full access.
CSV 101 — Foundation Course
A full 15-module course covering the complete CSV lifecycle. From system classification and risk assessment to testing, reporting, closure, and internal audit.
View Course DetailsArticles & Regulatory Watch
In-depth articles on common CSV challenges, plus monthly summaries of FDA warning letters and regulatory updates and what they mean for your validation work.
See MembershipRemote Consulting
Need hands-on support? Compval offers fixed-price remote assessments, validation documents and team training for regulated organisations.
Learn MoreNot sure where your system stands?
Try the free GxP Readiness Planner to see where your system stands today, or book a conversation about your specific situation.