Reduce the Risk Associated With Maintaining a Dietary Supplement Company

Dietary Supplement 21 CFR 111 Assessment

As part of your commitment to quality and safety, you want to ensure that your dietary supplement company complies with all relevant regulations. One key area of focus is the Current Good Manufacturing Practices (cGMP) for Manufacturing, Packaging, Labeling, and Holding Operations for Dietary Supplements, outlined in Title 21 of the Code of Federal Regulations, section 111.

This comprehensive assessment will guide you through the requirements to identify gaps in your manufacturing practices and procedures. . It will help you develop strategies for improving quality and safety within your manufacturing operations to reduce risks associated with product defects or incidents.

Why Use This Assessment

Identify gaps in your practices and procedures
Manage corrective action requests and resolutions
Avoid missing requirements
Retain compliance knowledge during employee turnover

This assessment provides an in-depth review of all relevant regulations and guidance documents.

See how easy it is to use Dietary Supplement 21 CFR 111 Assessment to fulfill your commitment to maintaining high food safety and sanitation standards for your dietary supplement company.