Mankind Pharma
Pharmazeutische, rezeptfreie und Verbrauchergesundheitsprodukte.
Mankind Pharma stellt in seinem Betrieb in Neu-Delhi Pharma-, OTC- und Verbrauchergesundheitsprodukte her. Das Unternehmen beliefert Kunden aus den Bereichen Einzelhandel, Industrie, Gesundheitswesen, Gastronomie und Export in seinen aufgeführten Hauptmärkten.
- Type
- brand seeking distribution
- Location
- New Delhi, India
- Founded
- 1995
- Website
- mankindpharma.com
- Categories
- Medizin- & Gesundheitsbedarf, Körperpflege
- Markets
- Indien, Vereinigte Staaten, Vereinigte Arabische Emirate, Südafrika
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-09 Domain registry record
- product-authorised-for-sale (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- cin-on-site (amber), checked 2026-08-30 Published on the company's own website
- 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)
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- fda-registered (green), checked 2026-08-09 FDA
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- customer-reviews (green), checked 2026-08-09 MouthShut
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
- FDA Registered FDA Establishment Registration
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- 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)