Credentials

Licensed and registered in the State of Qatar.

Wellspring Medical LLC holds all licences, registrations and memberships required to import, store, promote and distribute healthcare products across Qatar.

Wellspring Medical — official licences and registrations

Company registration

Full legal standing.

All registration details can be verified directly with the Ministry of Commerce and Industry at www.moci.gov.qa.

Verify at moci.gov.qa

Legal name: Wellspring Medical · ويل سبرينج الطبية
Legal form: Limited Liability Company
Commercial Registration: No. 192877
Commercial Licence: No. 304303
Issued by: Ministry of Commerce and Industry
Established: November 2023
Tax registration: General Tax Authority
Membership: Qatar Chamber of Commerce and Industry
Product regulator: Ministry of Public Health

Registration can be verified with the Ministry of Commerce and Industry at www.moci.gov.qa.

Registered commercial activities

Authorised to trade across the full healthcare spectrum.

The following activities are registered under Commercial Licence No. 304303.

Wholesale of pharmaceutical and medical goods

Wholesale of medical devices, equipment and supplies

Wholesale of medical appliances, perfumery and cosmetics

Retail sale of medical devices, equipment and supplies

Retail sale of pharmaceutical, medical and cosmetic goods in specialised stores

Trade of special and healthy food

Retail sale of medicinal herbs

Pharmaceutical and medicinal products warehouses

Quality and compliance

Built for principals who need certainty.

Wellspring operates a documented quality management system aligned with MOPH requirements, giving international manufacturers the assurance they need before appointing a Gulf distributor.

MOPH-aligned QMS

Written quality manual, SOPs and work instructions covering every operational process.

Cold-chain capability

Temperature-controlled storage and transport for products requiring 2–8 °C or 15–25 °C conditions.

Recall and complaint handling

Documented recall procedure, complaint log and adverse-event reporting to MOPH.

Regulatory affairs team

In-house expertise for MOPH dossier preparation, labelling review and post-registration variations.

Satisfied with our credentials?

We welcome due-diligence requests from international manufacturers. Send us your distributor questionnaire and we will respond within five business days.

Send a due-diligence request