Reviewing scientific literature to ensure therapy safety.Reporting adverse reactions as well as other safety issues encountered in medicinal products for a large range of pharmaceutical companies.

Taking part in the development of new medicinal products, food supplements and medical devices.Updating other company departments on projects advancement, through meetings or reporting.Identifying and contacting manufacturers of active substances and excipients.Presenting the company’s products during both local and national conferences for pharmacists and medicine and health professionals.

Drug registry files preparation, processing and updating, keeping track and analysis of drug policies among countries.Participating in the development of new products.Keeping up-to-date with Polish and European regulations on registration procedures for medicinal products, medical devices and food supplements.Searching and selecting a notified body to carry out certification of Farmina's medical devices. Cooperating in the creation of product information and their editing.