Register Now for online training to support annual GMP refresh and FSVP.
Virtual Training Focused on FDA Expectations.
GMP Fundamentals: Where Systems Commonly Break Down
Register by January 20, 2026
- Wednesday, January 21
- Virtual via Microsoft Teams
- 10 a.m MT / 11 a.m. CT / 12 p.m. ET
- 60 minutes. 45 presentation and 15 for live questions
- $79 per person, $350 per team (up to five)
Grounded Learning.
Meaningful Application.
Practical Execution.
Start 2026 grounded in GMP fundamentals with this practical, one-hour refresher designed for quality, regulatory, and operations teams in the dietary supplement, ingredient, and food industries.
This session focuses on what the FDA expects companies to write, implement, and execute well based on real inspection experience, not theory.
We will review common GMP gaps and practical expectations for specifications and manufacturing records during our January session.
In February, we will address supplier qualification, GMP documentation requirements, and how to assess whether your system is inspection-ready quickly.
The session is intentionally concise, low-cost, and actionable, with a live Q&A.
January Agenda:
- Overview of the most common GMP deficiencies and how to avoid them
- Specifications to meet GMP requirements
- Component and finished product expectations
- Common gaps that trigger FDA observations
- GMP Manufacturing Records
- Master Manufacturing Records (MMRs)
- Batch Records (BRs)
- Documentation expectations and practical pitfalls
To attend this training, please register using the link below. After payment of $79, you will receive the meeting invitation by email within 24 hours.
GMP Systems: Beyond the Basics
Register by February 10
- Wednesday, February 11, 2026
- Virtual via Microsoft Teams
- 10 a.m MT/ 11 a.m. CT/ 12 p.m. ET
- 60 minutes. 45 presentation and 15 for live questions
- $79 per person, $350 per team (up to five)
Grounded Learning.
Meaningful Application.
Practical Execution.
This practical, one-hour GMP refresher is designed for teams who want to ensure their policies, processes, controls, and systems are aligned with current FDA expectations.
We will review common GMP gaps and practical expectations for specifications and manufacturing records during our January session.
In February, we will address supplier qualification, GMP documentation requirements, and how to assess whether your system is inspection-ready quickly.
February Session Agenda
- Overview of the most common GMP deficiencies and how to avoid them
- Supplier Qualification in 2026 and aligned with GMPs
- Hazard Analysis and Food Safety Plans
- Verification Steps
- Foreign Supplier Verification Programs
- GMP documentation requirements & review
- There are ~30 documents the FDA investigator may ask for to demonstrate your system is operating in a state of control. Are you ready?
To attend this training, please register using the link below. After payment of $79, you will receive the meeting invitation by email within 24 hours.
Foreign Supplier Verification Programs (FSVP): A Practical Introduction for U.S. Importers
Register by February 24
- Wednesday, February 25
- Virtual via Microsoft Teams
- 10 a.m. MT / 11 a.m. CT / 12 p.m. ET
- 60 minutes. 45 presentation and 15 for live questions
- $79 per person, $350 per team (up to five)
Grounded Learning.
Meaningful Application.
Practical Execution.
Foreign Supplier Verification Programs (FSVP) is the #1 violation and most frequently cited FDA compliance gap for U.S. food importers, including companies importing ingredients and components used in dietary supplements. While FSVP has been in effect for several years, FDA inspection data and import enforcement trends show that many companies continue to misunderstand their responsibilities or underestimate the FDA expectations.
This 45-minute introductory session is designed to provide U.S. importers with a clear, practical overview of FSVP requirements, focusing on what FDA actually evaluates during inspections and record reviews. The session emphasizes common deficiencies, real-world expectations, and how FSVP fits into broader quality and supplier management systems.
Learning Objectives:
By the end of this session, participants will understand:
- Who is legally responsible for FSVP and how FDA determines the “importer”
- Why FSVP continues to be one of FDA’s top citation categories for food companies
- Core FSVP elements FDA expects to see in place and available at the time of inspection
- Common FSVP mistakes that lead to FDA observations or import delays
To attend this training, please register using the link below. After payment of $79, you will receive the meeting invitation by email within 24 hours.