Hamdard Laboratories (Waqf) Pakistan
Hamdard Laboratories (Waqf) Pakistán es uno de los laboratorios de medicina herbaria Unani más grandes del sur de Asia y...
Hamdard Laboratories (Waqf) Pakistán es uno de los mayores fabricantes de productos de bienestar y medicinas herbarias Unani del sur de Asia, y produce jarabe de Rooh Afza, tónicos de hierbas, mermeladas, miel y una amplia gama de medicinas tradicionales bajo la marca Hamdard. Con fabricación en Lahore y Karachi, la empresa exporta a más de 40 países, incluidos el Reino Unido, los Emiratos Árabes Unidos, Arabia Saudita y América del Norte, y abastece a distribuidores de comestibles de la diáspora e importadores de alimentos saludables.
- Type
- brand seeking distribution
- Location
- Lahore, Pakistan
- Founded
- 1948
- Website
- hamdard.pk
- Categories
- Bebidas, Suplementos y bienestar, Suministros médicos y sanitarios
- Markets
- Emiratos Árabes Unidos, Arabia Saudí, Reino Unido, Estados Unidos, Canadá, Australia
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)