Regulatory

• Having sufficient knowledge of drug registration rules & regulations for registration of products
• Adequately capability of registering new products in the Drug National List
• Well knowledge of the drug, raw material and food supplement approval process and registration bureaucracy in Ministry of Health
• Submitting registration documents to MOH

Manufacturing

We have ensured world-class quality in design, equipment and operations in our manufacturing facility. We have access to the state-of-the-art manufacturing sites near Tehran, Iran. This manufacturing units is located in Kaveh industrial zone, Saveh . Our units ensure that we are able to provide best-in-class products to patients across the Iran and emerging markets around.

Our manufacturing operations are focused on producing generics and branded generics, in the full range of dosage forms, including tablets, capsules, injectable, pre-filled syringe and freeze dried powder. We have a highly skilled team of regulatory affairs specialists who are well versed with regulatory policies and procedures in Iran. They have a wealth of experience in the timely filing of dossiers as well as handling regulatory queries from both authorities and customers.

Joint venture

By entering in Joint venture, ARANG will take advantage of the strong product portfolio, broad market outreach and experience with the production and commercialization of branded generic medicines. The joint venture will benefit from research and development (R&D), manufacturing quality management, international market promotion and operational capabilities. It will focus on R&D and the production & commercialization of high-quality branded generic medicines, and the broader commercialization of existing medicines through a local and global sales and marketing infrastructure. It will be operated in accordance with international quality standards to advance both companies’ mission of bringing high-quality and affordable medicines to address the medical needs of patients in Iran and worldwide.

Imports of Finished Pharmaceuticals

As the pioneer of our mission to meet the needs of the health society across IRAN and beyond with our expert staffs and facilities to import different health care products. With strong distribution network and reliance to our knowledge and experience in regulatory and medicine registration in Iran, together with our marketing team, we are capable to provide services from Commercial infrastructure, including pharmaceutical, registration, distribution, sales and marketing entirely for enthusiast’s pharmaceutical company around the world in order to enter to Iran pharma market.

Under the Iran MOH law a limited volume of medicines which are unregistered in Iran Drug List (IDL), and are dispensed at the responsibility of the general practitioner, are allowed to be imported. In order to meet the needs of patients to these rare or limited volume medicine in Iran pharma market ARANG attempt to import single- copy medicines to Iran.

Technology Transfer

We have the facilities in Iran to produce the medicine with high technology and we are open for technology transferring, work under the license and mutual development to produce highest standards & quality products.

R&D Department:

We in R&D department aimed to Reach to various market requirements and high quality products, by representing formulation and providing new method analysis, taking advantage of experienced Experts, using the most up to dated sources of pharmaceuticals and advanced devices. In addition to exploitation of cooperation and consultation of prominent University professors and other authentic science centers.