amgis lifescience ltd
Hindistan'da API Üreticisi - Veterinerlik ve İnsan Sağlığı API - AMGIS Lifescience Ltd.
AMGIS Lifescience, 30'dan fazla API, Veterinerlik API'si, İnsan Sağlığı API'si ve İlaç Ara Ürünleri üreten Hindistan'ın önde gelen ilaç üretim şirketlerinden biridir. Değerli müşterilerimizin güvenini kazandık ve Veteriner API'leri ve İnsan API'leri dünyasında Öne Çıkan Liderlerden biri olduk. Vapi, Surat, Ankleshwar, Ahmedabad, Hydrabad, Mumbai, Bangalore, Delhi ve Chennai'de bulunuyoruz.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Vapi, India
- Website
- https://www.amgislifescience.com
- Categories
- İlaç Üretimi, Takviyeler ve Sağlık
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)