Fermenta Biotech Ltd.
Pioneer manufacturer of Vitamin D3 and biotech-derived pharmaceutical ingredients.
Fermenta Biotech is a pioneer in manufacturing Vitamin D3 (Cholecalciferol) and other biotech-derived pharmaceutical ingredients. Its GMP-certified facility in Maharashtra uses patented fermentation technology to produce high-purity nutraceutical APIs. The company supplies to global health and nutrition companies.
- Type
- Manufacturer
- Location
- Mumbai, India
- Founded
- 1952
- Website
- https://www.fermentabiotech.com
- Categories
- Medical & Healthcare Supplies
- Markets
- United States, Germany, United Kingdom, Brazil, Japan
Verified facts
- customer-reviews (amber), checked 2026-08-08 MouthShut
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- market-access-eu (green), checked 2026-08-22 TRACES NT, European Commission register of approved establishments (DG SANTE)
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- export-registered (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- registered-manufacturer (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- Good Manufacturing Practice
- FDA Registered FDA Establishment Registration
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)