amgis lifescience ltd
インドの API メーカー - 獣医および人間の健康 API - AMGIS Lifescience Ltd.
AMGIS Lifescience は、30 以上の API、獣医用 API、ヒト健康用 API、医薬品中間体を生産しているインドの大手医薬品製造会社の 1 つです。当社は貴重なクライアントの信頼を獲得し、獣医用 API と人間用 API の世界で著名なリーダーの 1 つになりました。私たちはバピ、スーラト、アンクルシュワール、アーメダバード、ハイドラバード、ムンバイ、バンガロール、デリー、チェンナイに拠点を置いています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Vapi, India
- Website
- https://www.amgislifescience.com
- Categories
- 医薬品製造, サプリメントとウェルネス
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)