Clinical Data Management

Results: 1569



#Item
111Clinical research / Pharmaceutical industry / Clinical data management / Drug safety / Electronic common technical document / Supplementary protection certificate / European Medicines Agency / Summary of Product Characteristics / Pharmacovigilance / Validation / Drug Master File

DOC Document

Add to Reading List

Source URL: www.ema.europa.eu

Language: English - Date: 2016-07-20 07:22:57
112Explanatory Note Monitoring Questionnaires tool This tool may assist local authorities signing the Pact of Islands to collect and store useful data from the main activity sectors during the ISEAP implementation period. T

Explanatory Note Monitoring Questionnaires tool This tool may assist local authorities signing the Pact of Islands to collect and store useful data from the main activity sectors during the ISEAP implementation period. T

Add to Reading List

Source URL: www.sustainableislands.eu

Language: English - Date: 2015-06-08 12:28:44
11318 March 2015 EMAProcedure Management and Business Support Division Use of XML delivery file for submissions via eSubmission Gateway / Web Client – phased implementation for all

18 March 2015 EMAProcedure Management and Business Support Division Use of XML delivery file for submissions via eSubmission Gateway / Web Client – phased implementation for all

Add to Reading List

Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:16:00
114Attachment 8b 2014 Waterways Field Study: New V6 Crossings Report Project Note Project: Alaska Stand Alone Pipeline/ASAP

Attachment 8b 2014 Waterways Field Study: New V6 Crossings Report Project Note Project: Alaska Stand Alone Pipeline/ASAP

Add to Reading List

Source URL: asapgas.agdc.us

Language: English - Date: 2014-11-02 23:57:37
115Clinical research / Clinical data management / Pharmaceutical industry / Pharmaceuticals policy / Electronic common technical document / Common Technical Document / Marketing authorization / Validation / Pharmacovigilance / HTML element / Summary of Product Characteristics / European Medicines Agency

RTF Document

Add to Reading List

Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:15:41
116How to send submissions via the Web Client - User Guidance

How to send submissions via the Web Client - User Guidance

Add to Reading List

Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:15:47
117Microsoft Word - GS 016_Final Report Dora II_Mweb+Mee_Rev04_ Clean mode.doc

Microsoft Word - GS 016_Final Report Dora II_Mweb+Mee_Rev04_ Clean mode.doc

Add to Reading List

Source URL: www.project-climate.de

Language: English - Date: 2012-02-05 19:37:25
118PSUR Repository – MAH Training on new functionality Webinar training on new functionality provided in releasePresented by Kristiina Puusaari on 25 July 2016

PSUR Repository – MAH Training on new functionality Webinar training on new functionality provided in releasePresented by Kristiina Puusaari on 25 July 2016

Add to Reading List

Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:16:01
119Copernicus Land Monitoring Services – Validation of the Imperviousness HRL Summary of preliminary results 1. Context This summary report covers the validation of the High Resolution layer (HRL) on Imperviousness (IMD)

Copernicus Land Monitoring Services – Validation of the Imperviousness HRL Summary of preliminary results 1. Context This summary report covers the validation of the High Resolution layer (HRL) on Imperviousness (IMD)

Add to Reading List

Source URL: land.copernicus.eu

Language: English - Date: 2015-12-18 04:54:11
120Mandatory eCTD for Human centralised procedure ASMF submissions - Statement of Intent

Mandatory eCTD for Human centralised procedure ASMF submissions - Statement of Intent

Add to Reading List

Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:14:57