21 CFR Part 211 – Lead Auditor

This specialized training bundle prepares professionals to serve in the role of **21 CFR Part 211 Lead Auditor**. By completing both courses, trainees develop an understanding of Current Good Manufacturing Practice (CGMP) requirements for finished pharmaceuticals along with the principles and practices used to plan, conduct, and manage effective audits.

Successful completion of the bundle results in a 21 CFR Part 211 – Lead Auditor certificate, recognizing specialized training in auditing pharmaceutical manufacturing operations for compliance with applicable CGMP requirements.