PRODUCTION
MANUFACTURİNG FACILITIES IN TOPKİM A.Ş.
One of the main targets of our company is manufacturing veterinary pharmaceuticals, feed additives and premixes within various kinds of vetrinary field activities. One of our basic strategies is industrial manufacturing of specificly developed formulations, modern, innovative, efficient and reliable veterinary pharmaceuticals under accepted security procedures. Our company has modern facilities, scientific and technological framework, Professional work team including academicians and scientists which provide manufacturing of high technology-products as well as know-how activities. We are continuously following a long-term Schedule regarding R&D studies in remarkable success.
There are all kinds of necessary technological equipments and manufacturing units in our manufacturing site in order to produce different kinds of pharmaceuticals in various types and formulations which are commonly being used in veterinary field. In this qualified, efficient manufacturing site, injectible solutions, suspansions, powders, oral-solutions, emulsions, suspansions and tablets, intra-mammary products and liquid disinfectants are being manufactured. In our Topkapı site; insecticid preparations are manufactured based on EC solution and pour on solution in a seperate unit. There are quality control labs and premix manufacturing units producing with computerized dosages and formulations. All these products are being preferred not only in Turkey but also worldwide in different foreign countries because of their high quality and efficiacy.
Quality Control : Manufacturing qulified, efficient, reliable and economic pharmaceuticals and premixes is our basic principle of our company. Required efforts are put forward in order to keep the well known quality and continuous manufacturing process without any cocession. Qualified staff have been working in high tech and equipped quality labs since our foundation.
We are respectfully applying Good Manufacturing Procedures ( GMP ) and Good Laboratory Practices ( GLP ) of the European Pharmacope and European Union’s Medical Evaluation Agency ( EMEA ) with respect to in process controls during the manufacture of pharmaceuticals. These mentioned scientific and lawful control items are certain basic applications for producing qualified pharmaceutics.
Both our sales team in the field and our R&D Department are closely and continuously following up the products from the point of view of products stability, efficiacy and possible negative cahnges in the pharmaceutical form as they are kept in our ware houses or at he veterinarians’ place after manufacturing and submission to the market. Such that, all kinds of requests and comments are being evaluated by our quality control labs and R&D Department group.
