Glenmark Pharmaceuticals
Thuốc generic có thương hiệu, thuốc đặc trị và apis.
Glenmark Pharmaceuticals sản xuất thuốc generic, thuốc đặc trị và API có thương hiệu từ các hoạt động ở Mumbai. Công ty cung cấp cho khách hàng bán lẻ, công nghiệp, chăm sóc sức khỏe, dịch vụ thực phẩm hoặc xuất khẩu trên các thị trường chính được liệt kê.
- Type
- brand seeking distribution
- Location
- Mumbai, India
- Founded
- 1977
- Website
- glenmarkpharma.com
- Categories
- Vật tư y tế và chăm sóc sức khỏe
- Markets
- Ấn Độ, Hoa Kỳ, Đức, Brazil
Verified facts
- domain-registered (green), checked 2026-08-02 Domain registry record
- product-authorised-for-sale (green), checked 2026-08-23 Rwanda FDA, register of registered human medicinal products
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- 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)
Claimed certifications
- Good Manufacturing Practice
- FDA Registered FDA Establishment Registration
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)