Gulshan Polyols Ltd.
Grain-based ethanol and industrial minerals
Gulshan Polyols manufactures grain-based ethanol, sorbitol, and processed mineral powders for the food, pharma, and industrial sectors. Its ISO 9001 and HACCP-certified plants in Uttar Pradesh and Gujarat produce high-purity ingredients. The company is a major supplier of non-GMO ethanol and mineral extenders.
- Type
- Manufacturer
- Location
- Delhi, India
- Founded
- 1981
- Website
- https://www.gulshanpolyols.com
- Categories
- Pantry & Dry Goods, Medical & Healthcare Supplies
- Markets
- United States, United Kingdom, United Arab Emirates, Bangladesh
Verified facts
- domain-registered (green), checked 2026-08-12 Domain registry record
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- debarment-clear (green), checked 2026-08-12 OpenSanctions
- sanctions-clear (green), checked 2026-08-12 OpenSanctions
- 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
- HACCP
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- 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)