Making the Transition to Digital GAMP 5 Validation

Digitalizing traditional pharma quality management processes is considered a risky move. Sticking with old paper-based methods is even riskier. Download this guide to modernizing quality management & collaboration in pharma systems validation!

A guide to digitalizing pharma quality management and collaboration

The pharmaceutical industry is experiencing huge technological changes. Still, paper-based document management continues to be the standard and accepted way of managing collaboration, quality documentation, and systems validation. This ‘digital inertia’ presents a variety of challenges – but also means opportunities for companies willing to consider going digital.

This eBook serves as a guide for pharmaceutical end users, system integrators, and suppliers of automated systems to support them on their journey to achieving digital maturity. This guide analyzes the challenges of paper-based process validation and lists the benefits of transitioning to a modern digital approach.

To help navigate the process digitalization landscape, the eBook also contains a step-by-step guide to digitalizing GAMP systems validation. The final section provides an overview of available tooling options to support the transition. Download this eBook for a comprehensive guide to digitalizing pharma quality management and collaboration!

Download this eBook for insights about:

  • The challenges of paper-based process validation in pharma
  • A step-by-step guide to digitalizing Good Automated Manufacturing Practices systems validation
  • Tooling decisions when moving away from paper-based processes

Your download is sponsored by Intland Software.