Whether your business operates a laboratory, clinic or pharmaceutical manufacturing line, GxP is essential.
Resource
GxP toolkit
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
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 manufacturersLearn 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 checklistMeet every e-record and e-signature FDA requirement with our step-by-step checklist
The business case for electronic
GxP managementSee why more and more GxP businesses are turning to integrated quality management software tools for robust and automatic GxP.