List of Sessions

Date
Session Type
Session Date
21 CFR 111 Dietary Supplement GMP Overview - Part 2 178
Attend an extensive 2-day training course on 21 CFR 111, the current Good Manufacturing Practices (cGMPs) in manufacturing, and packaging, labeling, or holding operations for dietary supplements. This course is geared to those individuals involved in the ...
Dietary Supplement Label Compliance 180
It is up to dietary supplement manufacturers to ensure their supplement labels are compliant before they go to market, however the regulations can be confusing and difficult to interpret. Label noncompliance can cause your product to be considered misbranded ...
Root Cause Analysis (Investigative and Justification Writing) 179
In this training, we will address non-conformance report (NCR), CAPA and problem report (PR) writing. We will cover thorough root cause analysis writing and demonstrate how to write clear investigations that flow, identify real root cause(s), implement ...
Vendor Qualification and Audit Training 181
This course is designed to give people who want to improve quality in their facility and who already have a basic understanding of the Dietary Supplement GMPs, the knowledge and skills necessary to qualify suppliers. Since the evaluation of all types of ...
21 CFR 111 Dietary Supplement GMP Overview - Part 1 169
Attend an extensive 2-day training course on 21 CFR 111, the current Good Manufacturing Practices (cGMPs) in manufacturing, and packaging, labeling, or holding operations for dietary supplements. This course is geared to those individuals involved in ...
Dietary Supplement Claim Substantiation 173
The labeling and promotion of your dietary supplement products are the most visible ways that the Food & Drug Administration and the Federal Trade Commission can track your compliance with federal regulations. A perfect complement to “Dietary Supplement ...
FDA Inspection Readiness for Dietary Supplements 172
Preparing for an FDA inspection for dietary supplements will help you avoid getting a warning letter and the regulatory and business consequences that come with it. Establishing a relationship of professional trust between you and the FDA requires preparation ...
ISO 22716 GMP’s for Cosmetics and Personal Care Professionals 174
The ISO 22716 GMP cosmetics training will show you how to identify regulatory non-compliances before they become an issue, minimizing risk while adding measurable value to the manufacturing process. This course has been updated with information from the U.S. ...