GMP Fundamentals
Good Manufacturing Practice Training for Regulated Industry Teams
Practical compliance, not just theory.
What This Training Covers
Current Good Manufacturing Practice (cGMP) training built for the people who work in regulated manufacturing environments every day — not just quality managers. This workshop translates 21 CFR Parts 110, 111, and 211 into practical, scenario-based learning that sticks. Teams leave with a shared understanding of what GMP requires, why it matters, and how to apply it in their specific facility.
Who this is for
Production supervisors, quality technicians, warehouse and receiving staff, operations managers, and any team member who works in or around a regulated manufacturing environment. Ideal for new hire onboarding, annual refresher training, and pre-audit preparation.
Topics Covered
- GMP regulatory framework — 21 CFR Parts 110, 111, and 211 in plain language
- Personnel hygiene, gowning, and facility access controls
- Equipment cleaning, maintenance, and qualification basics
- Raw material receipt, sampling, and release procedures
- Batch records, logbooks, and documentation best practices
- Deviations, investigations, and CAPA fundamentals
- Environmental monitoring and contamination control
- Common GMP audit findings and how to prevent them
Delivery Formats
Half-Day Workshop
Condensed core GMP fundamentals for teams with limited availability. Ideal for refresher training or focused onboarding of new production staff.
Full-Day Workshop
Comprehensive coverage including scenario exercises, facility walk-through review, and documentation practice. Recommended for new facility launches and pre-audit preparation.
Private On-Site
Delivered at your facility using your actual SOPs, batch records, and equipment as training materials. Maximum relevance, minimum abstraction.
Applicable Regulatory Frameworks
- 21 CFR Part 110 — Current Good Manufacturing Practice in Manufacturing, Packing, or Holding Human Food
- 21 CFR Part 111 — Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements
- 21 CFR Part 211 — Current Good Manufacturing Practice for Finished Pharmaceuticals
- FDA Guidance for Industry — Quality Systems Approach to Pharmaceutical cGMP Regulations
- ICH Q10 — Pharmaceutical Quality System (for pharma-adjacent operations)
Ready to Schedule GMP Training?
We deliver this workshop at your facility, tailored to your products, processes, and regulatory environment. Contact us to discuss your team's needs and schedule.