This is a summary of the European public assessment report (EPAR) for Qutenza. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Qutenza.
Qutenza : EPAR - Summary for the public (PDF/75.69 KB)
First published: 12/11/2009
Last updated: 08/10/2015
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|Date of issue of marketing authorisation valid throughout the European Union||
28/01/2021 Qutenza - EMEA/H/C/000909 - II/0051/G
- Annex I - Summary of product characteristics
- Annex IIA - Manufacturing-authorisation holder responsible for batch release
- Annex IIB - Conditions of the marketing authorisation
- Annex IIIA - Labelling
- Annex IIIB - Package leaflet
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