Electronic common technical document

Results: 446



#Item
41Annex 2 to the HMA eSubmission Roadmap: Implementation of mandatory eCTD format for regulatory submissions (Status: Final version adopted by the eSubmission CMB. Dated 26 JulyScope This annex is intended for both

Annex 2 to the HMA eSubmission Roadmap: Implementation of mandatory eCTD format for regulatory submissions (Status: Final version adopted by the eSubmission CMB. Dated 26 JulyScope This annex is intended for both

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Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:15:41
42BAP_Guidance_v1 0_June 2013

BAP_Guidance_v1 0_June 2013

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Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:16:06
43Clinical research / Clinical data management / Electronic common technical document / Agencies of the European Union / Pharmaceuticals policy

23 June 2016 EMAversion 1.1 Periodic Safety Update Report (PSUR) repository mandatory use: questions and answers Information for Marketing Authorisation Holders on how to submit a PSUR 1. What is the PSUR r

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Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:16:04
44Updated 08 JulyRelease Notes Detailing the updates of the EU eCTD Module 1 Specification The published version 3.0 has been updated to versionto correct pick list values and the updated version was publishe

Updated 08 JulyRelease Notes Detailing the updates of the EU eCTD Module 1 Specification The published version 3.0 has been updated to versionto correct pick list values and the updated version was publishe

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Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:15:41
45E-submission-GL- VerSeptember 15

E-submission-GL- VerSeptember 15

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Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:16:07
46Implementation guide for EU eCTD M1 specification

Implementation guide for EU eCTD M1 specification

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Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:15:42
47Clinical research / Clinical data management / Pharmaceutical industry / Electronic common technical document / Pharmaceuticals policy / Common Technical Document / Marketing authorization / ASMF / European Medicines Agency / European Directorate for the Quality of Medicines / Dossier / Electronic submission

Revision version 1.5 for public consultation Comments byJune 2016

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Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:14:57
48E-Submission Guideline - Jan 2013

E-Submission Guideline - Jan 2013

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Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:16:06
4922 JulyJuly 2016 EMAv7.0 User Guidance for Marketing Authorisation Holders (MAHs) for PSUR Repository

22 JulyJuly 2016 EMAv7.0 User Guidance for Marketing Authorisation Holders (MAHs) for PSUR Repository

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Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:16:02
50FebruaryError codes If your submission was unsuccessful you will be able to find out the reason for this by viewing the error code inside the acknowledgement message. The error codes below reflect common errors wh

FebruaryError codes If your submission was unsuccessful you will be able to find out the reason for this by viewing the error code inside the acknowledgement message. The error codes below reflect common errors wh

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Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:14:56