(Two-day course): NSF/ANSI 455-2 for dietary supplement manufacturing standard part 1
Information
The purpose of this training is to understand the requirements for the NSF/ANSI 455-2 good manufacturing practice (GMP) for dietary supplement standard. GMP encompasses a set of guidelines that ensure consistent quality and safety in product manufacturing. This standard – which aligns with current good manufacturing practice (cGMP) and GMPs in the dietary supplement industry – is based on FDA regulations, specifically 21 CFR Part 111 requirements, other regulations (normative references), retailer criteria and industry best practices. The criteria in this standard were structured to follow a seven (7) systems approach to ensure comprehensive GMP compliance in the dietary supplement industry. In this training, we will discuss how to prepare for an audit at your dietary supplement manufacturing facility.
We will not be discussing the need for documented procedures and evidentiary records in depth, as this is well documented within the standard – as well as the prerequisite dietary supplement GMP training – and is always best practice for quality assurance (QA) and quality control (QC).
This course is geared to those individuals involved in the dietary supplement industry, including:
- Manufacturing
- Quality control/quality assurance
- Management
- Laboratory operations
- Packaging and labeling
- Auditing
- Suppliers and distributors
- Regulatory affairs and compliance
- Other technical professional
Additional fee required.
