Tag: pharma validation SOPs

Deciding When to Revalidate Using QRM Principles

Deciding When to Revalidate Using QRM Principles How to Decide When to Revalidate Using Quality Risk Management (QRM) Principles Revalidation in the pharmaceutical industry is essential for maintaining a consistent, GMP-compliant, and validated state of processes, systems, and equipment. However,…

Documenting Equipment Qualification in Pharma: Templates, Records & Audit Readiness

Documenting Equipment Qualification in Pharma: Templates, Records & Audit Readiness Documenting Equipment Qualification in Pharma: Templates, Records & Audit Readiness In the pharmaceutical industry, equipment qualification is not just about installation, operation, or performance testing. What distinguishes a compliant, audit-ready…