Companies
EAS Consulting Group
operates a network of more than 200 independent regulatory consultants providing 21 CFR Part 111 GMP audit preparation, batch-record development and labeling-compliance review across dietary supplements, food, drugs, medical devices and cosmetics.
- Country
- United States
fda-audit-prep
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Coverage
| CN | EU | US | |
|---|---|---|---|
| market-access-commercial | — | ✓ | ✓ |
| regulatory-legal | ✓ | ✓ | ✓ |
Regulatorsefsafdanmpa
Technologies
| Name | Cluster | Risk | |
|---|---|---|---|
| Feed-additive authorization (EFSA FEEDAP, FDA GRAS) | market-access-commercial | Low | → |
| GMP consulting for nutraceuticals | regulatory-legal | Low | → |
Compiled by BIOECON from primary sources.
Compliance
Bioecon is an information intermediary; it is not a regulator, a certification body, or a legal advisor. When working with public-sector customers (procurement under 44-FZ / 223-FZ), Bioecon acts solely as an independent analytical platform, with no remuneration from suppliers.