Pharmacovigilance

Direct Healthcare Professional Communication

This page contains the chronological overview of Direct Healthcare Professional Communications, which contain information concerning safe use of medicinal products.

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How to Report an Adverse Drug Reaction

Seal for Marking of Important Safety Information

In case of sending Dear Healthcare Professional Letters containing important safety information, which are prepared in collaboration with HALMED, marketing authorisation holders should place a seal prepared by HALMED on the front side of an envelope. Its purpose is to additionally emphasize the importance of information in the envelope.

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Submission of Application Documentation for Assessment of Non-Interventional Trials

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Submission of Safety Information in Clinical Trials of Medicinal Products

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New Safety Information

This page contains news concerning activities in the area of pharmacovigilance.

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Risk minimisation measures (RMM)

This page contains an overview of medicinal products with Risk Minimisation Measures (RMM) granted by HALMED. RMMs are additional measures introduced for certain medicines, the application of which is associated with specific risks - therefore they cannot be authorised without such measures.

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List of serious adverse reactions

On this page you can access the list of adverse reactions considered to be serious, but are not unambiguously determined according to the seriousness criteria stipulated in Guideline on Good Pharmacovigilance Practices (GVP) Module VI, as well as inclusion and exclusion criteria for this list.

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Adverse Drug Reactions Reports

On this page you will find a chronological overview of Annual Reports on Spontaneous Reporting of Adverse Drug Reactions in Croatia, published regularly by HALMED.

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Signal management

A safety signal is information on a new or known adverse event that is potentially caused by a medicinal product and that warrants further investigation.

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SCOPE Project

On this page you will find information on participation of HALMED in the project of European Commission "Joint Action on Strengthening Collaboration for Operating Pharmacovigilance in Europe (SCOPE)".

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Rapid ALERT SYSTEM

Registry Office

Important information

Ksaverska cesta 4, Zagreb
Customer service: 8.00 a.m. to
3.30 p.m.

Before submitting more applications, please make an announcement at + 385 1 4884 162, +385 1 4884 165, +385 1 4884 106

E-mail:

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