Pharmacovigilance

Pharmacovigilance is a process of collecting, monitoring, searching and evaluating of information provided by health care professionals and patients in order to detect and prevent problems related to the use of medicines. Our quality experts are responsible for collecting, monitoring, evaluation of information and reporting on the safety of the treatment of current pathologies.

In accordance with the international requirements of Directive 2001/83/EC of the European Parliament and the Council and  Regulation (EC) No. 726/2004 of the European Parliament and local legislation of the countries, in the markets of which the products are represented, the manufacturer of medicines must carry out objective and proper monitoring of safety of the medicines it produces. In this regard, our company has its own pharmacovigilance system.

The process of pharmacovigilance begins at the stage of drug development and continues throughout its life cycle. Timely detection of adverse events is key to the safety of medicines. It is important for the company to maintain effective feedback from you.

If you or your patients have any questions connected with the pharmaceuticals of CROWN   FARMA and its products, please, contact us at + 380 (44) 303 91 40.

We will send your questions to our experts to conduct a qualitative analysis of the primary information received in order to give qualified answers.