Aani Darman Co was registered in 2014 in affiliation with Ahran Group which is considered as one of the largest Iranian pharmaceutical groups and obtained establishment license in 2018 during march 2019 was officially authorized to implement their solid oral dosage forms production line (Tablet and Capsule) Aani Darman was granted the GMP certificate from the Iranian FDA after inspection and meeting with their approval and is prepared for and capable of contract manufacturing and analysis. The primary duty of every pharmaceutical manufacturer is to ensure the safety and efficacy of their products at all stages of preparation - before and after market entry. The Quality Control Department of Aani Darman supported by the continuous supervision of the experienced management and the effective effort of expert employees keeps assessing the manufactured products and helps provide high quality products. Our QC Department consists of microbial control laboratories device analysis in process quality control (IPQC) packaging control physicochemical control of raw materials and products units. Our laboratories located in an appropriate area designed and equipped with advanced equipment according to the latest FDA quality control guidelines and international standards. The mission of all staff is to pay special attention to safety focusing on the quality of the manufactured products environmental protection human organizational and community values education innovation improvement and to help raising the health level and awareness of the community which contribute to the high quality of Aani Darman Products.