Medicines and ingredients for Iran, sourced and registered by one team.

Hanpars imports active ingredients, finished medicines, excipients and nutrition ingredients, and registers them with the IFDA. Based in Tehran, with suppliers in Türkiye, China, India and Europe.

Prepare a sourcing enquiryRegulatory affairs
Hanpars medicines on the display shelves at the Tehran office
Finished dosage forms46 registered medicines and 626 reference products.Active ingredients1,453 substances in the reference range.Excipients1,832 excipients, by grade and specification.Nutrition ingredients267 authorised EU health claims.

Three things we do, usually together.

A supply agreement is only useful once the product is approved and on the shelf, so sourcing, registration and project coordination sit with the same people.

Import and sourcing

APIs, excipients and finished products from manufacturers we already work with, brought into Iran with the certificates and stability data the authority expects.

API reference range

Regulatory affairs

CTD, eCTD and ACTD dossiers, IFDA and TİTCK submissions, authority correspondence and lifecycle maintenance. On its own, or with the products we supply.

What we cover

Development partnerships

For finished dosage-form projects we coordinate development and manufacturing partners, with responsibilities written down at the start. We run the project; partners run the plant.

How a project begins

The hospital and specialty portfolio

46medicines registered with the IFDA
30available in Iran
16launching

Contrast media, anaesthetics, antibiotics, hormones and biologics from GMP-certified manufacturers, distributed nationally through Pakhsh Razi, Darougostar Tooba and Dey Darou Omid. Hanpars is a contracted supplier to the national Strategic Medicine Reserve.

See the portfolioRepresent your products in Iran

Status as of October 2026; confirm availability when you enquire.

Tehran beneath the snow-covered Alborz mountains
شرکت هانیا پرسان دارو

A trading company in Tehran that holds its own licences.

Hanpars is the marketing authorisation holder for the medicines it imports: the dossier, the IRC licence and pharmacovigilance are handled in-house. We source, register and coordinate; manufacturers manufacture, and the authority decides. Saying precisely who does what is how we keep projects moving.

Haniya Parsan Darou Co. · 3rd floor, No. 326, Zafar Street, Africa Boulevard, TehranOffice hours 09:00–17:00 · +98 21 8888 3325
About Hanpars

How a request proceeds

A product name and a destination are enough to start.

  1. Tell us what you need

    The product, the strength or grade, the quantity and where it is going.

  2. We put it in context

    Who can supply it, what the market will require, and what is realistic for timing.

  3. We agree the scope

    Who does what, in writing, with one contact at Hanpars accountable for it.

From the archive

All archived articles

Dated editorial commentary, not a current forecast or regulatory advice.

Tell us the product and the market. We will tell you the next step.

Send the molecule or ingredient, the specification and the destination. We reply from Tehran with the questions, the documents and the next step.

Prepare a sourcing enquiryDiscuss regulatory or CDMO support
Telephone+98 21 8888 3325 · office hours 09:00–17:00, Tehran
OfficeHaniya Parsan Darou, 3rd floor, No. 326, Zafar Street, Africa Boulevard, Tehran 1968734974, Iran
Emailcontact@hanpars.com