"Croatia ready for action on EU medicines regulation front"
On the occasion of Croatia’s accession to the EU and the integration of the Agency for Medicinal Products and Medical Devices (HALMED) as a full member of the European regulatory network, an interview with Dr. Viola Macolić Šarinić, MD, PhD, clinical pharmacologist and toxicologist was published in July 2013 in Scrip Regulatory Affairs.
In the interview, Dr. Macolić Šarinić emphasised the importance of the pre-accession preparations in medicines regulation undertaken by HALMED in time. The article presents changes in medicines regulation in Croatia, as well as activities of medicines regulation in which HALMED wants to take part and thus contribute to the new regulatory environment.
Article download (Scrip Regulatory Affairs, July 2013.)
