<--- Back to Details
First PageDocument Content
Medicine / Food and Drug Administration / Medical informatics / Clinical Data Management / Pharmaceutical industry / Clinical Data Interchange Standards Consortium / Clinical investigator / Center for Biologics Evaluation and Research / Electronic Common Technical Document / Pharmaceutical sciences / Clinical research / Research
Medicine
Food and Drug Administration
Medical informatics
Clinical Data Management
Pharmaceutical industry
Clinical Data Interchange Standards Consortium
Clinical investigator
Center for Biologics Evaluation and Research
Electronic Common Technical Document
Pharmaceutical sciences
Clinical research
Research

Data Standards Strategy – Action Plan Version: 1.1 Document Date: July 29, 2013

Add to Reading List

Source URL: www.fda.gov

Download Document from Source Website

File Size: 121,59 KB

Share Document on Facebook

Similar Documents

TIGes vet Q&A-update - Sept 2013

TIGes vet Q&A-update - Sept 2013

DocID: 1rsZK - View Document

Updated 08 JulyRelease Notes for the EU eCTD Validation Criteria version 6.1 The currently valid version of the eCTD validation criteria is version 6.1 and it needs to be applied as of 1 July 2016 in combination w

Updated 08 JulyRelease Notes for the EU eCTD Validation Criteria version 6.1 The currently valid version of the eCTD validation criteria is version 6.1 and it needs to be applied as of 1 July 2016 in combination w

DocID: 1rlRj - View Document

Release Notes for Harmonised Technical Guidance for eCTD Submissions in the EU v3.0 This document highlights the changes incorporated in version 3.0, in comparison with version 2.0, of the eCTD guidance document. For cle

Release Notes for Harmonised Technical Guidance for eCTD Submissions in the EU v3.0 This document highlights the changes incorporated in version 3.0, in comparison with version 2.0, of the eCTD guidance document. For cle

DocID: 1rj2G - View Document

1 AugustElectronic Application Forms are now fully available for use For initial marketing authorisation (human and veterinary), variation and renewal applications

1 AugustElectronic Application Forms are now fully available for use For initial marketing authorisation (human and veterinary), variation and renewal applications

DocID: 1riM4 - View Document

Submissions to the PSUR Repository using EMA Gateway/Web Client

Submissions to the PSUR Repository using EMA Gateway/Web Client

DocID: 1rhRl - View Document