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Romania - specific requirements Print E-mail
Regulatory Affairs - Romania
Written by Zdravko Mauko   
Thursday, 19 April 2007
Article Index
Romania - specific requirements
Page 2
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NUMBER OF COPIES OF THE DOSSIER, RESPONSES, VARIATIONS AND RENEWALS

National and Mutual Recognition applications 

NtA vol. 2.B (Edition 1998)

CTD (Modules)

RO

Full dossier

Full dossier

172

Additional

Module 1.1

-

Additional Part IA

Module 1.2

2

Additional: IB, SPC, Leaflet, etc.

Module 1.3.1

Module 1.3.2

Module 1.3.3

 

2

 

Module 1.3.4

1

 

Module 1.3.5

3

Additional: IC Expert Reports

Module 1.4

-

 

Module 1.5

-

 

Module 1 - Annex

-

 

Module 2

1

Additional: Part II

Module 3

3

Additional: Part II for Biological/Biotech.

Module 3 for Biological/Biotech.

-

Additional: Part III

Module 4

1

Additional: Part IV

Module 5

-

Written responses

 

273

Variations

 

 

Application form

 

2

Type I Documentation

 

174

Type II Documentation

 

174

Supplementary info

 

-

Additional SPC/Leaflet

 

-

Additional Labels

 

-

Additional statement on Qualitative & quantitative Composition

 

-

Written responses

 

273

………………….

………………..

72 1 paper copy of full dossier + 1 copy on CD-ROM + 1 paper copy for Module 1, only for MRP/DP

73  The written response should be bound in separate volumes so that pharmaceutical assessor can review the response to Part I and II (CTD 1, 2, 3), the pre-clinical assessor the response to Part I and III (CTD 1, 2, 4) and the clinical assessor the response to Part I and IV (CTD 1, 2, 5)

74 An electronic version of SPC and PIL in RO in word format, with track changes for variations



Last Updated ( Saturday, 24 May 2008 )
 
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