About Us

DarmanYab Salamat Pouya Co. (DYSP) was established in 2010 to work specially on importing medical equipment. This company was at fist a business unit within DarmanYab Darou during 5 years before it has been established but as this emergent business unit was growing remarkably fast using Darmanyab Group infrastructures, DYSP has been established as a company and member of DY group. With over a decade of experience in medical market as an independent department, DYSP focus on providing better customer support on points of sales to increase customers’ satisfaction level.

The strength and competitive advantages of DYSP are the results of its successful experience in business development, branding, marketing, after-sales-services, education and distribution of medical products in Iran. We are proud of our team for introducing new technology and concepts to Iranian market.

The company is exclusively representing a collection of world leading international medical and dental equipments with successful records. DYSP has been affiliated with a network of specialized marketing and distribution companies as well as its service points. It has also dedicated distribution network (DYPA) which is located throughout the country and provides excellent market coverage.

The success of DYSP is the result of meeting the expectations of all stakeholders and close cooperation with customers such as Ministry of Health, hospitals, healthcare Professionals, academic institutes, pharmacies and medical shops.

DYSP emphasizes strongly on educational & scientific approaches in Technical Support, Sales & Marketing, Education and trainings, Business Development and Supply Chain Management. Each business division participates in local and international exhibitions as well as conducting regular dedicated workshops and training courses for customers, key opinion leaders and end-users.

Darman Yab Salamat Pouya Co. has acquired ISO 9001 (quality management system standard), ISO 13485 (quality management system for the design and manufacture of medical devices) and ISO 10002 (guidance on the process of complaints handling related to products within an organization).