Appendix III to the qrd templates for human medicinal products



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3 February 2016

EMEA/29277/2003 v.4

Human Medicines Evaluation Division

Appendix III to the QRD templates for human medicinal products

This appendix should be read together with the Note for Guidance on the Declaration of Storage Conditions A) in the product information of medicinal products, and B) for active substances (EMEA/CPMP/QWP/609/96/Rev 2).

The purpose of the Note for Guidance is to set out uniform statements on storage conditions for inclusion in the product information of medicinal products and labelling of active substances and to define when they apply. The CHMP adopted a revision of this document in November 2007, which resulted in amendments of/or additions to the required storage statements.



Storage Conditions

BG Bulgaria

IT Italian

CS Czech

LT Lithuanian

DA Danish

LV Latvian

DE German

MT Maltese

EL Greek

NL Dutch

EN English

NO Norwegian

ES Spanish

PL Polish

ET Estonian

PT Portuguese

FI Finnish

RO Romania

FR French

SK Slovak

HR Croatian

SL Slovenian

HU Hungarian

SV Swedish

IS Icelandic





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© European Medicines Agency, 2018. Reproduction is authorised provided the source is acknowledged.




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