The Regulatory Affairs department at Nikan Pharmed is headed by a qualified pharmacist and includes several other experts with substantial knowledge of pharmaceutical regulations.

After years of professional work experience, they have attained sufficient expertise to proceed with the speedy registration, import, and even export of medical products in compliance with the laws and regulations of the Iran Food and Drug Administration and the Ministry of Health.

Despite stringent regulatory laws set by the governing authorities, Nikan's regulatory team has successfully registered and imported more than 35 high-tech pharmaceuticals, including niche products, Foods for special medical purposes (FSMPs), Biopharmaceuticals, emergency, and prescription-based products from reputable manufacturers and suppliers worldwide.

To facilitate the regulatory processes concerning product registration and import, our regulatory team is in close touch with the regulatory bodies to obtain up-to-date information regarding the import and registration of medicines especially those which fall under the emergency import category.

In addition, our regulatory team has succeeded in the speedy registration and import of prescription-based products to help those with rare diseases access the appropriate medicine with high quality at a reasonable cost in the shortest possible time.