Virtual Training Focused on FDA Expectations.

GMP Fundamentals: Common GMP Breakdowns & Potential Solutions

Register by April 14, 2026

Wednesday, April 15

Virtual via Microsoft Teams
10 a.m. MT / 11 a.m. CT / 12 p.m. ET

60 minutes total
45-minute presentation + 15-minute live Q&A

$79 per person | $350 per team (up to five)

Grounded Learning.
Meaningful Application.
Practical Execution.

Learn the top FDA citations and how we can do better as an industry.

GMP Fundamentals is a focused, one-hour workshop built for quality, regulatory, and operations teams in dietary supplements, ingredients, and food.

This is not theory.

This session is based on real FDA inspection experience and what investigators actually look for, where systems break down, and what triggers observations.

You’ll walk away with a clear understanding of what needs to be written, what needs to be supported, and what needs to work in practice.

What we will cover

The most common GMP breakdowns seen during inspections
What FDA expects for specifications - component and finished product
Where companies consistently fall short (and how to fix it)
Practical approaches you can apply immediately

Why this session works

Concise and high-impact (no filler)
Built from real inspection experience
Immediately applicable to your systems
Live Q&A to address your specific challenges

To attend, register using the link below.

After payment, you will receive your Microsoft Teams invitation within 24 hours.

Larisa Pavlick giving a presentation at SupplySide China 2018.

Foreign Supplier Verification Programs (FSVP): A Practical Introduction for U.S. Importers

Wednesday, May 27
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.

GMPs Required Records & Written Procedures. The expectations and how to be prepared

June 17, 2026, at 10 MT

You see it in FDA Warning Letters often citing failure to establish written procedures for returns, complaints, recalls, quality responsibilities, and more. Did you know that during an FDA inspection, I requested about 31 records?

These are not just records. They will help your facility meet GMP expectations and may actually improve efficiency.

Join us to help your team master GMP written procedures & Manufacturing Records (Specifications, Master Manufacturing Records, Batch Records) like a pro. This session is designed for dietary supplements and dietary ingredients.

We will cover what you need to know and what the FDA expects to help you prepare and modernize your GMP records.

Wednesday, June 17
Virtual via Microsoft Teams
10 a.m. MT / 11 a.m. CT / 12 p.m. ET
90 minutes. One-hour presentation and at least 20 minutes for live questions and discussion
$79 per person, $350 per team (up to five)

GMP Training

Manufacturing Documentation, Written Procedures, Specifications & FDA Enforcement

Focus: Compliance with 21 CFR Part 111 (Dietary Supplement cGMPs) for supplements

Core Themes: Written procedures: SOPs, Master Manufacturing Records (MMRs), Batch Production Records (BPRs), and enforcement expectations.

In this focused 90-minute introductory session, we break down the core regulatory requirements for written procedures and GMP Records and explain how the FDA evaluates them during inspections.

It’s a practical walk-through of what the FDA expects to see and where companies most often struggle, paired with supportive, real-world strategies to help you build stronger, inspection-ready systems with confidence.

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. Fill the conference room with your team rate: $350.

At Haven, GMP also means:

Get it.

Make it.

Prove it.

What does GMP mean to your business?

Mastering the Art of Dietary Supplement Specifications

Register by July 15, 2026

Wednesday, July 14

Virtual via Microsoft Teams
10 a.m. MT / 11 a.m. CT / 12 p.m. ET

Specifications are a foundational element of GMP systems and one of the most common areas of FDA findings.

This practical session focuses on how to build clear, defensible specifications for dietary supplements, grounded in real inspection experience. We will cover FDA expectations, the “GMP Big Five,” and common gaps that lead to observations, along with practical approaches you can apply immediately.