In 2006, the second GMP approved production facility and in 2007, the third GMP approved production facility and the production of human medicine products were expanded;in the form of solid dosage forms and aseptically produced injection solutions.
In the following decades, it has begun to produce competitive prescription qualities and to produce pre-filled syringes and medicinal products in the form of perfusion solutions.
Rompharm Company has taken the decision to manufacture medicinal products for human consumption for the Turkish pharmaceutical market in parallel with production, sales and marketing operations carried out in Europe and CIS countries.
At the end of 2015, Rompharm Pharmaceutical started production operations in our GMP approved production facility of Ministry of Health of Turkey.
Our production facility located in Çerkezköy Organized Industrial Zone Tekirdag has 4 production lines where sterile injectable solutions and medicinal products for human use in the form of sterile eye drops are produced.
The total production capacity of our facility is 130 million units / year. The licensing studies of injectable solutions and generic products in the form of eye drops, which we aim to present to the Turkish pharmaceutical market, continue at a rapid pace.
In our ophthalmic medical products market in Turkey, it is our primary goal to provide the first and second generic equivalent products that will be an alternative to the original products in the treatment areas such as glaucoma, ocular hypertension, eye infection and ophthalmia as soon as possible and to provide public benefit.
As an international pharmaceutical company, our priority is to maintain the quality, ethical standards and honesty provided at all production, sales and marketing operations we carry out at a high level.