In order to optimize the production line and maintain the quality of products in a long period of time, manufacturing companies under the supervision of the Iran Food and Drug Administration should enforce and implement guidelines under the title of Good Manufacturing Practice. In fact, GMP is a system to ensure that manufactured products are always produced and controlled in accordance with “pre-determined” standards, legal requirements and specifications. GMP principles are defined to minimize risks that cannot be eliminated simply by testing the final product.

Industries such as pharmaceuticals, cosmetics, health and food are required to use chemicals that are produced under GMP rules and under the supervision of legislative organizations due to the importance and high sensitivity of their nature of work. In line with international standards, DRM has pursued the following goals by obtaining a GMP certificate from the Food and Drug Administration of the Ministry of Health:

• Fulfilling the in house file creation for completion of customers documentations.
• Reassuring consumers of long term and constant services in terms of maintaining the quality of products.

The production lines, warehouses and laboratories of this company are periodically visited and audited by inspectors of the Food and Drug Administration and experts and GMP auditors of other pharmaceutical companies. In addition, many of our customers can also visit the different departments of this company (including the laboratory, (Arak and Saveh factories) and get to know the capabilities of this complex. DRM, proudly invites all of you, dear customers, artisans and professors, to visit this complex and familiarize yourself with the capabilities of this company, and make us learn from your valuable guidance and experiences with us.
DRM, believes: the quality of a product depends on the quality of the people who produce it.