Razak laboratories with around 50 years of efficient experiences in manufacturing human and veterinary medicines and also veterinary feed supplements has been considered as a reputable pharmaceutical company in IRAN. The company not only observes GMP guidelines and other national and international standards, but also considers quality as its most important mission. Additionally it has been the first drug manufacturer which could get ISO 9001 certificate from TÜV NORD for all its products.
This section consists of 6 departments inclouding sterile Dept (veterinary vial), Solid Dept (tablet & capsule), liquid Dept (oral syrup), semi solid Dept (ointment and jell), veterinary supplement Dept and Packaging Dept. APIs (Active Pharmaceutical Ingredients) and Excipients are weighed in Raw material warehouse in presence of the warehouse supervisor, a production representative and under supervision of a QC representative, so after entering the production unit a pharmacist get them weighed again to be verified for being produced.
In 2007 the Company decided to establish and run a sterile Dept in veterinary field by investing in development of production Areas regarding GMP guidelines, so it has been producing sterile veterinary vials since then.
Furthermore, manufacturing of β-lactam injectable antibiotics and also cephalosporins is our future plan. This new selection is designed according to clean room standards of liquid and powder vials. All processes from production to filling will be performed automatically without human interference. CIP & SIP will be done every day and after each production.