Whether your business operates a laboratory, clinic or pharmaceutical manufacturing line, GxP is essential.
Download our GxP toolkit to:
- Understand the essentials of GxP, from GAMP to ALCOA+ data integrity
- Start taking actionable steps towards business-wide GxP
- Meet the requirements of FDA 21 CFR Part 11
Complete the form to the right to get started!
What you'll get
- GxP compliance checklist
Follow step-by-step guidance to ensure you meet the '5 Ps' of GxP compliance
- Guide to GAMP 5 and data integrity for GxP manufacturers
Learn how to assess and interrogate your manufacturing system and data flows for weak spots - then take the right steps to an integrated quality by design (QbD) approach
- FDA Title 21 electronic records & signatures guide
Understand how to meet modern electronic record GxP demands, keep the FDA happy and follow ALCOA+ principles.
- FDA 21 CFR Part 11 compliance checklist
Meet every e-record and e-signature FDA requirement with our step-by-step checklist
- The business case for electronic GxP management
See why more and more GxP businesses are turning to integrated quality management software tools for robust and automatic GxP.