Ancalima Lifesciences Ltd
Nhà sản xuất quy mô nhỏ đã đăng ký Pharmaxcil, Ấn Độ
Ancalima Lifesciences Ltd là thành viên của Pharmexcil, Hội đồng Xúc tiến Xuất khẩu Dược phẩm Ấn Độ (Bộ Thương mại và Công nghiệp). Hội đồng đăng ký công ty này là nhà sản xuất quy mô nhỏ, đây là cách phân loại riêng của hội đồng chứ không phải suy luận của chúng tôi.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- India
- Founded
- 1994
- Website
- https://ancalima.com
- Categories
- Sản xuất dược phẩm
- Markets
- Ấn Độ
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
- product-authorised-for-sale (green), checked 2026-08-20 NAFDAC Greenbook, Nigeria - register of authorised products (manufacturer named on the authorisation)
- 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
- 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
- export-registered (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- registry-activity (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
Import rules for these goods
- 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)