Hamdard Laboratories (Waqf) Pakistan
Hamdard Laboratories (Waqf) Pakistan è uno dei più grandi laboratori di medicina erboristica Unani dell'Asia meridionale e ben ...
Hamdard Laboratories (Waqf) Pakistan è uno dei maggiori produttori di prodotti erboristici e per il benessere Unani dell'Asia meridionale, che produce sciroppo Rooh Afza, tonici a base di erbe, marmellate, miele e un'ampia gamma di medicine tradizionali con il marchio Hamdard. Con la produzione a Lahore e Karachi, l'azienda esporta in oltre 40 paesi tra cui Regno Unito, Emirati Arabi Uniti, Arabia Saudita e Nord America, rifornendo distributori di generi alimentari della diaspora e importatori di alimenti naturali.
- Type
- brand seeking distribution
- Location
- Lahore, Pakistan
- Founded
- 1948
- Website
- hamdard.pk
- Categories
- Bevande, Integratori e benessere, Forniture medicali e sanitarie
- Markets
- Emirati Arabi Uniti, Arabia Saudita, Regno Unito, Stati Uniti, Canada, 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)