amgis lifescience ltd
مُصنع API في الهند - API للطب البيطري والصحة البشرية - AMGIS Lifescience Ltd.
AMGIS Lifescience، هي إحدى شركات تصنيع الأدوية الرائدة في الهند التي تنتج أكثر من 30 واجهة برمجة تطبيقات، وواجهة برمجة تطبيقات بيطرية، وواجهة برمجة تطبيقات صحة البشر، ووسيطات فارما. لقد اكتسبنا ثقة عملائنا الكرام وأصبحنا أحد القادة البارزين في عالم واجهات برمجة التطبيقات البيطرية وواجهات برمجة التطبيقات البشرية. نحن موجودون في فابي، سورات، أنكليشوار، أحمد أباد، حيدر أباد، مومباي، بنغالور، دلهي، وتشيناي.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Vapi, India
- Website
- https://www.amgislifescience.com
- Categories
- تصنيع الأدوية, المكملات الغذائية والعافية
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)