GxP toolkit

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

  1. GxP compliance checklist
    Follow step-by-step guidance to ensure you meet the '5 Ps' of GxP compliance

  2. 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

  3. FDA Title 21 electronic records & signatures guide
    Understand how to meet modern electronic record GxP demands, keep the FDA happy and follow ALCOA+ principles.

  4. FDA 21 CFR Part 11 compliance checklist
    Meet every e-record and e-signature FDA requirement with our step-by-step checklist 

  5. 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.


GxP compliance toolkit