Practitioner-led · Not textbook-driven
Real-world Good Manufacturing Practice training for pharmaceutical, dietary supplement, cosmetics, and food manufacturers — taught by Jared Clark, CPGP, a consultant who implements GMP systems for a living. On-site workshops and live online courses, built from what FDA inspectors actually look for.
ASQ Certified Pharmaceutical GMP Professional — plus CQA, CMQ-OE, RAC, JD, MBA.
Course material drawn from real audits, real 483 observations, and real remediations — not hypotheticals.
Pharmaceutical (21 CFR 210/211), supplements (Part 111), cosmetics (MoCRA/ISO 22716), and food (Part 117).
Custom workshops at your facility, or live virtual instructor-led sessions for distributed teams.
Every program is scoped to your operations, your product category, and the regulation that actually governs you — then delivered on-site or live online.
21 CFR 210/211, API cGMP, validation, laboratory controls, data integrity, inspection readiness.
View program →21 CFR Part 111 — identity testing, MMRs and BPRs, quality operations, holding & distribution.
View program →MoCRA-era GMP expectations and ISO 22716 — covered inside the cGMP course catalog.
View catalog →21 CFR Part 117 current GMPs, sanitation, allergen controls, and training documentation.
View catalog →Most GMP training comes from institutions — universities, standards bodies, big course platforms. Their material teaches the regulation as written. It rarely teaches what happens when an FDA investigator sits down with your batch records.
GMP Training Institute is different by design: every module is built by a consultant who spends the rest of the week implementing GMP systems, hosting inspections, and remediating 483 observations for real manufacturers. The examples are real. The documentation habits are the ones that survive inspections. The questions your team asks get answered by someone who has seen the failure modes first-hand.
Jared Clark — JD, MBA, PMP, CMQ-OE, CQA, CPGP, RAC
Principal Consultant at Certify Consulting and holder of ASQ's Certified Pharmaceutical GMP Professional credential. Jared doesn't just teach GMP — he implements it, with 200+ client engagements across pharmaceutical, supplement, cosmetics, and food manufacturing. His legal training (JD) adds the regulatory "why" that makes the "how" stick.
At your facility, on your lines, with your SOPs. Best for onboarding whole teams and inspection-readiness pushes.
Instructor-led over video, fully interactive, with the same documentation package. Ideal for distributed or multi-site teams. Online training details →
Annual training plans, refresher curricula, and role-based tracks designed around your quality system and audit history.
GMP training teaches employees of regulated manufacturers how to follow Good Manufacturing Practices — the FDA regulations (21 CFR 210/211 for drugs, Part 111 for supplements, Part 117 for food) that govern how products are made, tested, documented, and released. It's an explicit regulatory requirement, not a nice-to-have.
Everyone engaged in manufacturing, processing, packing, testing, or holding a regulated product — from line operators to the quality unit. Inspectors routinely pull training records, and "inadequate training" is a recurring 483 theme.
FDA's language is "on a continuing basis." In practice: onboarding training, a defined refresher cycle (annual is the norm), and event-driven training when procedures change or deviations reveal gaps. Your program defines it; your records prove it. See what 21 CFR 211.25 actually requires →
Yes — the regulations require that training happen and be documented, not that it happen in a classroom. Our live virtual sessions deliver the same curriculum and the same documentation package as on-site workshops.
Programs are scoped to team size, industry, and format — an on-site workshop for fifty operators prices differently than a virtual refresher for a five-person quality unit. Tell us about your team and you'll get a concrete quote, not a rate card surprise.
Tell us your industry, team size, and compliance deadline. We'll design a GMP training program around your operations — and document every minute of it.