amgis lifescience ltd
인도의 API 제조업체 - 수의학 및 인간 건강 API - AMGIS Lifescience Ltd.
AMGIS Lifescience는 30개 이상의 API, 수의학 API, Humans Health API 및 의약품 중간체를 생산하는 인도 최고의 제약 제조 회사 중 하나입니다. 우리는 귀중한 고객의 신뢰를 얻었으며 수의학 API 및 인간 API 세계에서 저명한 리더 중 하나가 되었습니다. 우리는 Vapi, Surat, Ankleshwar, Ahmedabad, Hydrabad, Mumbai, Bangalore, Delhi 및 Chennai에 위치하고 있습니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Vapi, India
- Website
- https://www.amgislifescience.com
- Categories
- 의약품 제조, 보충제 및 웰니스
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-04 Mail server of the company domain
- domain-registered (green), checked 2026-08-04 Domain registry record
- web-presence-since (green), checked 2026-08-02 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- export-registered (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registry-activity (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)