21 CFR 111 Dietary Supplement GMP Overview Intro: Q&C Training Event
June 24 – 25, 2021
21 CFR 111 Dietary Supplement CGMP Overview Intro: 2 Part instructor Led Remote Training
This course provides an overview of 21 CFR 111, the Dietary Supplement CGMPs. This abridged course includes an introduction to current good manufacturing practices (cGMPs), required product quality elements, documentation, investigations and a brief overview of the relevant subparts. We will also review the proper way to execute GMP records, detail the personal hygiene requirements, examine the meaning of master and batch records for control of production, labeling and packaging, clarify the requirements of quality and, describe the purpose of GMP rules, regulations and FDA enforcement.
o Buildings and Facilities
o Facility Records
o Production and Process Control
o Holding and Distribution
o Batch Records
o Packaging and Labeling
o Quality Control and Quality Assurance
o Laboratory Operations
o Product Complaints
· The role of the FDA and their authority
· The roles and responsibilities of the Quality Unit
As a part of maintaining compliance to 21 CFR 111, dietary supplement personnel must have GMP training on a regular basis.
Day 1: Thursday June 24, 2021 1:00 P.M to 5:00 P.M Eastern Time
Day 2: Friday June 25, 2021 1:00 P.M to 5:00 P.M Eastern Time
In order to receive a certificate of completion/participation you must be in attendance 95% of the log in time. Attending NSF training sessions does not provide an advantage, nor is it linked in any way to the granting of certification. Course log in details will be sent in a separate email.
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Introduction to Vendor Qualification for Dietary Supplements- Recording 1
Dietary Supplement Claims Substantiation Training 1
Top 10 Audit Findings and Ways to Get a Warning Letter