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National Medicines Agency of Romania has published country specific requirements for MRP and DCP 

Useful  information abut specific requirements related to Romania are available.

LANGUAGES TO BE USED FOR DOSSIER, RESPONSES, VARIATIONS AND RENEWALS

National and Mutual Recognition applications 

Dossier

CTD

RO

 

Module 1.1

RO/EN

Part IA - Format

Module 1.2

RO/EN

Part IB - SPC

Module 1.3.1

RO/EN15

Part IB – Leaflets & Labels

Module 1.3.2 – 1.3.4

RO/EN16

 

Module 1.4

RO/EN

 

Module 1.5

RO/EN

 

Module 1 - Annex

RO/EN

Part IC – Expert Reports

Module 2

RO/EN

Part II

Module 3

RO/EN17

Part III

Module 4

RO/EN

Part IV

Module 5

RO/EN

Written responses

 

RO/EN

Variations

 

 

Application form

 

 

Type I Documentation

 

RO/EN

Type II Documentation

 

RO/EN

Written responses

 

RO/EN

Renewal

 

RO/EN

………………….

………………..

15 EN for MRP/DCP and RO for national procedures. An electronic version (EMEA template) is also required

16 RO for Module 1.3.2 and Module 1.3.3 and EN for Module 1.3.4

17 An electronic copy, preferably in word format is also required

 


 
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