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Rates advice KOAGKAG
The Netherlands Keuringsraad KOAGKAG can be consulted for advice with regard to promotional material and claims taking into account the current codes and guidelines for medicinal products, medical devices and health products. As the complexity of the questions...
Announcement of changes in EU pharmacovigilance legislation
Europe In December 2024, a draft version of an amendment to the European legislation for pharmacovigilance activities (Implementing Regulation EU No. 520/2012) has been published by the European Commission. Public feedback was collected until the 15th of January 2025....
New European regulation for Health Technology Assessment
Europe The new European Health Technology Assessment (HTA) regulation came into force in January. The main goals of this EU HTA regulation (EU HTAR) are: to improve and speed up the availability of innovative medicines and medical devices to patients across the EU; to...
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Terloonststraat 22
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Belgium
info@in2pharma.com