Hamdard Laboratories (Waqf) Pakistan
Hamdard Laboratories (Waqf) Pakistan est l'un des plus grands laboratoires de phytothérapie Unani d'Asie du Sud et bien…
Hamdard Laboratories (Waqf) Pakistan est l'un des plus grands fabricants de plantes médicinales et de produits de bien-être Unani d'Asie du Sud, produisant du sirop Rooh Afza, des toniques à base de plantes, des confitures, du miel et une large gamme de médicaments traditionnels sous la marque Hamdard. Avec une production à Lahore et Karachi, l'entreprise exporte vers plus de 40 pays, dont le Royaume-Uni, les Émirats arabes unis, l'Arabie saoudite et l'Amérique du Nord, approvisionnant les distributeurs d'épicerie de la diaspora et les importateurs d'aliments naturels.
- Type
- brand seeking distribution
- Location
- Lahore, Pakistan
- Founded
- 1948
- Website
- hamdard.pk
- Categories
- Boissons, Compléments et bien-être, Fournitures médicales et de santé
- Markets
- Émirats arabes unis, Arabie saoudite, Royaume-Uni, États-Unis, Canada, Australie
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-06 Mail server of the company domain
- registry-id-verified (green), checked 2026-08-19 FBR Active Taxpayer List (Federal Board of Revenue, Pakistan)
- registered-manufacturer (green), checked 2026-08-19 Pakistan Standards and Quality Control Authority (PSQCA), register of valid Certification Mark licences (local manufacturer scheme)
- sanctions-clear (green), checked 2026-08-06 OpenSanctions
- debarment-clear (green), checked 2026-08-06 OpenSanctions
Claimed certifications
- Halal Certified
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- 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)
- 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)