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Qdossier Qsauri
"P"

procedure
Guideline or reference source
TIGES Harmonised guidance for ectd submissions in the eu
Definition
A Community registration procedure for the authorisation of medicinal products in the European Community. There are 4 types of procedure that operate within the EC – Centralised, Decentralised, Mutual Recognition and National.
Use
marketing authorization procedure
 

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