21 CFR Part 111 cGMP Training — Built for U.S. Dietary Supplement Compliance

Start in minutes. Train at your own pace. One-year access with ongoing quizzes and certification to support FDA inspections and cGMP compliance under 21 CFR Part 111.

Register Why This Training

WHY THIS TRAINING

Built for Ongoing Dietary Supplement cGMP Compliance

Under 21 CFR Part 111, companies must ensure personnel are qualified through appropriate training. Training must be maintained and documented as part of ongoing cGMP compliance.

This program is designed to support these requirements through structured, practical training aligned with real-world operations.

  • Aligned with FDA 21 CFR Part 111
  • Supports refresher training and onboarding
  • Supports cGMP documentation requirements

REGULATORY AUTHORITY

Built Around Real cGMP Compliance Requirements

This training is developed by dicentra’s regulatory and quality experts who support dietary supplement companies with cGMP compliance, FDA requirements, and inspection readiness.

Insights from working with companies across manufacturing, packaging, labeling, and holding operations are built directly into the training.


Includes a focus on:

  • Common cGMP gaps and risks
  • Documentation and evidence expectations
  • Practical cGMP implementation across operations
  • Personnel qualification and training requirements

WHAT THE TRAINING COVERS

Full Coverage of 21 CFR Part 111 (Subparts A–P)

Comprehensive coverage of all subparts supporting full cGMP understanding.

Overview of cGMP requirements and regulatory scope.

Training, qualifications, and hygiene requirements.

Facility design, maintenance, and cleanliness.

Equipment requirements, cleaning, and calibration.

Establishing compliant production systems.

Quality unit responsibilities and oversight.

Control of incoming materials and labeling.

Requirements for creating and maintaining MMRs.

Documentation of batch-level production activities.

Testing and verification requirements.

Process controls during production.

Controls for packaging and labeling activities.

Storage and distribution requirements.

Handling and evaluation of returns.

Complaint handling and investigation.

Documentation retention and accessibility.

Who This Training Is For

This program is designed for professionals accountable for cGMP compliance across dietary supplement operations, including:

  • Quality Assurance Persons (QAPs)
  • QA / QC and Regulatory Affairs professionals
  • Importers, manufacturers, packagers, labelers, and distributors
  • Organizations preparing for upcoming cGMP inspections
  • Foreign sites manufacturing Dietary Supplements for the U.S. market

ONLINE FORMAT

Online Training Designed for Real-World Teams

cGMP compliance is not a one-time activity. This online training program supports ongoing training, documentation, and compliance across teams and locations.

Format Benefits:

  • On-demand access — train anytime, at your own pace
  • Supports remote and distributed teams
  • Progress tracking and completion records
  • Centralized oversight for QA and management

What’s Included

  • Comprehensive coverage of all subparts supporting full cGMP understanding 
  • 12-month access per registered user 
  • Complete dietary supplement cGMP online training program 
  • On-demand modules with structured learning paths 
  • Real-life inspection scenarios
  • Quizzes throughout to support learning and retention 
  • Final exam to validate understanding 
  • Personalized certificate
  • Unlimited re-access for refreshers during access period 
  • Quarterly refresher quizzes to support ongoing compliance

CERTIFICATION

Recognized Proof of cGMP Training

Each participant who successfully completes the training receives a personalized cGMP training certificate.

Certificates are designed to support internal compliance documentation and demonstrate cGMP training completion across teams and operations.

Includes:

  • Certificate issued upon successful completion of final assessment

  • Unique authenticity identifier for verification

  • Suitable for internal cGMP training records

  • Supports audit and inspection readiness

Widely Used To Support:

  • cGMP training records

  • Inspection readiness and audit preparation

  • Internal compliance documentation

Registration

  • 12-month access per registered user
  • Per-user pricing applies for 1–5 users
  • Contact us to purchase seats for 6+ users at a discounted rate
  • Enterprise options available for organizations with 100+ users

Register Contact Us for Enterprise Options

FAQ

Click to below to expand

  • Is this training aligned with FDA requirements?

    Yes. This training is structured around 21 CFR Part 111 and reflects current cGMP requirements for dietary supplements in the U.S.

  • Who should complete dietary supplement cGMP training?

    Personnel involved in manufacturing, packaging, labeling, holding, quality, and regulatory functions - including QAPs, QA/QC and Regulatory Affairs professionals, importers, distributors, and foreign manufacturers supplying the U.S. market.

  • How long do users have access?

    Each registered user receives 12-month access, including unlimited re-access during that period for refresher use.

  • Is the training self-paced?

    Yes. The training is fully online and can be completed at the user’s own pace.

  • Will participants receive a certificate?

    Yes. Each participant who successfully completes the training and final assessment receives a certificate as proof of training.

  • Does each certificate include a unique identifier?

    Yes. Each certificate includes a unique authenticity identifier to support internal documentation and verification.

  • Can this training be used for refresher training?

    Yes. The program is designed to support refresher training, onboarding, and ongoing cGMP compliance documentation.

  • Does this training replace regulatory or legal advice?

    No. This training is provided for educational purposes only and does not replace formal regulatory or legal advice.

  • When does the early-bird pricing end?

    The early-bird pre-registration offer expires on April 30, 2026.

What our customers say
Trusted by quality and regulatory professionals looking for practical, flexible cGMP training.

Paula

“I did this training for years, and now it’s more detailed. There’s a lot more to know. I really liked it because it was very straightforward and easy to follow.”

Michael

“This training has opened the door to many new job opportunities.”

Debbie

“It’s more convenient. It is easier for us. We have four facilities that cannot gather in one place for training. To hire somebody to do training for four sites is too expensive.”

Martin

“It is an easy way for us to train all of our employees, and it’s available to us 24/7. It’s also great for new employee orientation."

Rachael

“This has made such a difference to how we train our teams. Everything is in one place, and people can learn at their own pace. It’s taken a lot of pressure off our managers.”

Tom

“It’s practical, flexible, and easy to use. We’ve seen a real improvement in staff confidence since introducing it, especially with new starters getting up to speed much quicker.”

Regulatory Notice

This training is provided for educational purposes and does not replace formal regulatory or legal advice.