Medicinal Product Utilisation in Croatia from 2009 to 2013
Publication contains a comparative report on utilisation of medicinal products in the Republic of Croatia in the period from 2009 to 2013.
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News and Educations
Medicinal Product Utilisation in Croatia from 2007 to 2012
This HALMED's project is the first publication in Croatia containing a comparative report on medicinal product utilisation over a multiannual period, which can serve as basis for planning of utilisation of medicinal products and rational pharmacotherapy at all healthcare levels.
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The Clinical Trial - A Manual for Patients and their Families
Implementation of clinical trials is regulated by a number of laws and regulations, as well as by ethical standards. This manual is an opportunity to inform patients in greater detail of such regulations, methods of conducting clinical trials and their role in development of medicinal products, in a concise yet sufficiently informative way.
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Brochure: Safe use of medicinal products
How to detect and report an adverse reaction
The role and importance of healthcare professionals
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Brochure: Medicinal Products and the Internet
The information about medicines and medical advices that are accessible on the Internet, as well as broad spectrum of medicinal products offered for online purchase constitute numerous risks. The main problem is the enormous amount of accessible information and a large number of extremely suspicious offers.
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"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.
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Report to the European Commission on Pharmacovigilance audit carried out in 2013
On 17 September 2013 the Agency for Medicinal Products and Medical Devices (HALMED) submitted a report to the European Commission about the internal audit of its pharmacovigilance system for the period between 1 July and 16 September 2013.
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Report to the European Commission on Pharmacovigilance audit carried out in 2015
On 21 September 2015 the Agency for Medicinal Products and Medical Devices (HALMED) submitted a report to the European Commission on the internal audit of its pharmacovigilance system for the period between 16 September 2013 and 21 September 2015.
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Report to the European Commission on Pharmacovigilance audit carried out in 2017
On 19 September 2017 the Agency for Medicinal Products and Medical Devices (HALMED) submitted a report to the European Commission on the internal audit of its pharmacovigilance system for the period between 21 September 2015 and 19 September 2017.
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Report to the European Commission on Pharmacovigilance audit carried out in 2019
On 12 September 2019 the Agency for Medicinal Products and Medical Devices (HALMED) submitted a report to the European Commission on the internal audit of its pharmacovigilance system for the period between 19 September 2017 and 12 September 2019.
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