60 mins

How to Write Effective Standard Operating Procedures (SOPs)

How to Write an Effective Equipment User Requirement Specification (URS)

21 CFR Part 820 Subpart F – Identification and Traceability

An Introduction to Cleaning Validation

An Introduction to Process Validation – Part 2

21 CFR Part 820 Subpart C – Design Controls

The Life Cycle of a Software Validation Protocol

How to Prepare for Internal & External Laboratory Audits

How to Perform Supplier Qualification

Laboratory Investigations & Deviations