DIETARY SUPPLEMENTS COMPLIANCE ATTORNEYS
There is a myth among consumers that dietary supplements in the United States are wholly unregulated. Dietary supplements are subject to regulation under the Dietary Supplement Health and Education Act of 1994 (DSHEA) and various state laws. The Food and Drug Administration (FDA) is charged with regulating dietary supplement products in the United States.
Any company that manufactures, packages, labels, or holds a dietary supplement must comply with the Current Good Manufacturing Practices (cGMP). Compliance is of tantamount importance, as the FDA can pursue enforcement actions against any adulterated or misbranded dietary supplement.
Why Choose Us for Dietary Supplement Compliance?
Our dietary supplement team handles a wide range of compliance matters, including:
- FDA/DSHEA compliance
- New dietary ingredient notifications submissions;
- Product label and packaging review;
- Advertising review, including claims review;
- Structure/function claim advisement;
- Form 483 Response
- FDA Warning Letter Response
- Advising on all aspects of product labeling and advertising
- Developing permitted product claims with respect to structure/function
- Advising regarding nutrient content claims and health claims
- False, misleading, or deceptive advertising claims;
- Commercial contracts;
- Trademark registration.
Contact Ritter Spencer Cheng!
Proactive strategic planning can minimize or prevent risk for your dietary supplement business and prevent FDA enforcement actions. Our experienced regulatory is prepared to assist from product development to litigation. Contact Ritter Spencer Cheng PLLC today to schedule a consultation.