US Food and Drug Administration (FDA) regulations protect the health, safety, and overall quality of products so they do not adversely affect consumers. That is also why current good manufacturing practices (cGMP) are in place.
These requirements ensure the methods, equipment, facilities, and controls for manufacturing, packaging, and distributing dietary supplements are regulated.
NSF Health can help you keep up with these constantly-evolving requirements through its training programme or third-party GMP facility registration.
The advantages of third-party GMP facility registration:
- Provides peace of mind toward meeting FDA regulations
- Prepares you for potential FDA inspections
- Allows gaining trust among your customers that your facility runs a safe and high-quality operation
- Ensures qualification of your suppliers
- Grants you access to a partner that will assist your supplement brand through correctional procedures and marketing strategies
- Provides peace of mind toward meeting FDA regulations
- Prepares you for potential FDA inspections
- Allows gaining trust among your customers that your facility runs a safe and quality operation
- Ensures qualification of your suppliers
- Grants you access to a partner that will assist your supplement brand through correctional procedures and marketing strategies
How NSF stands above the rest
- Provides access to a global network of auditors and public health professionals
- Programme developed to meet federal expectations of the FDA’s 21 CFR Part 111 regulation compliance for dietary supplement cGMPs
- Implements two comprehensive audits each year to ensure continued compliance
- Grants access to an innovative online system for resolving any non-conformances found within a facility during an audit
- Supports promoting your facility’s GMP registration
NSF’s comprehensive training approach goes beyond content delivery. Its instructors’ extensive industry expertise provides tangible, real-world case studies of workplace situations and one-on-one interaction.