- 483, Warning Letter and Consent Decree remediation
- Internal and vendor audits
- Employee training
- Contamination control
- Material control
- Warehouse temperature/humidity control (including mapping)
- Analytical support (assay development and validation)
- Equipment qualification
- Cold chain management
About NutraReg LLCNutraReg LLC is dedicated to providing the Dietary Supplement industry with the tools and knowledge required to be compliant with US Food and Drug Administration (FDA), European Union (EU), and International Organization for Standardization (ISO) regulations and guidelines.
Our corporate office is located in Scotch Plains, NJ, with consultants located in the US, Canada, South America, Europe, China, and India.
In 2007, the FDA issued new Good Manufacturing Practices (GMPs) for Dietary Supplements (21 CFR Part 111) defining the regulatory compliance responsibilities for all Dietary Supplement companies that manufacture, package and/or distribute their products within the US.
NutraReg LLC provides support and guidance to Dietary Supplement companies of all sizes in complying with these new regulations that are quite similar to pharmaceutical GMPs.
We are now listed in the Natural Products Buyers Guide. Please see our listing under consulting, training and recruiting.
NutraReg will be exhibiting at the following conferences:
Javits Center, NY, NY
June 2-3, 2014