| |
Bringing 25 years of regulatory, industry
and scientific experience to your business
- Contract Research Organization (CRO)
- FDA regulatory compliance for supplements, foods and cosmetics
- FTC product advertising and marketing compliance
- Label review for FDA compliance with DSHEA requirements
- GLP toxicology testing of products for safety substantiation
- GCP clinical trial oversight for efficacy/safety substantiation
- Dietary supplement formulation development and upgrading
- GRAS self-affirmation determination
|
|
- New Dietary Ingredient (NDI) submissions to FDA
- Global product and market intelligence
- Raw material/ingredient sourcing world-wide
- Advice and counsel on strategic partnerships and mergers
- Publication of papers/articles in scientific and trade journals
- Technical assistance from highly qualified personnel
- Timely and responsive day-to-day technical support
- International and domestic product placements
- Supplementology®*
|
Contact us to benefit from this
experience >>
*U.S. Patent and Trademark Office registered No. 3,238,405 for,
“Technical consultation in the field of research, development and formulation of nutraceutical, botanical and natural preparations.”
|
|
