Marketing Authorization Application - PDFSEARCH.IO - Document Search Engine

Marketing Authorization Application
Results: 43

#	Item
1	1 AugustElectronic Application Forms are now fully available for use For initial marketing authorisation (human and veterinary), variation and renewal applications Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:40 Pharmaceuticals policy Health Medical research Clinical data management Clinical research Pharmaceutical industry European Union EudraLex European Medicines Agency Electronic common technical document Common Technical Document Marketing authorization
2	28 September 2015 EMAInformation Technology Electronic Application Form Data Exchange Standard 3.0 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:35 RDM Stage lighting Marketing authorization European Medicines Agency Health Government
3	Instructions for submitting Off Campus Authorization Requests 1. Access the UGA Russ Application in a web browser by going to russhelp.uga.edu 2. Click the link in the left hand navigation area called “Log into RUSS” Add to Reading List Source URL: russhelp.uga.edu Language: English - Date: 2014-02-27 09:37:28 Business Professional studies Economy User interface techniques Distribution Manufacturing Supply chain management Inventory Marketing Uga Point and click Form
4	GUI-010 Duplicate applications in MRP-DCPEMA-CMDv Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-06-15 05:38:48 Pharmaceuticals policy Pharmaceutical industry Marketing authorization Pharmacology Pharmaceutical sciences Patent application Health policy
5	01 June 2015 EMAInformation Technology Electronic Application Form Data Exchange Standard 3.0 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:30 RDM Stage lighting Marketing authorization Maa European Medicines Agency Health Government
6	7th June 2016 EMAInformation Technology Electronic Application Form Data Exchange Standard 3.0 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:32 RDM Stage lighting Maa Marketing authorization E21
7	Practical Guidance For the Paper Submission of Regulatory Information in Support of a Marketing Authorisation Application When Using an eCTD or a NeeS as the Source Submission. v2.0 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:14:51 Clinical research Clinical data management Electronic common technical document Pharmaceutical industry Pharmaceuticals policy Common Technical Document Marketing authorization Electronic submission Drug Master File
8	Application for grant of a Supplementary Protection Certificate for a Medicinal Product Danish Patent and Trademark Office Add to Reading List Source URL: iprights.dkpto.org Language: English - Date: 2016-05-17 05:21:58 Law Foreign relations Government Pharmaceutical industry Intellectual property law Marketing authorization Pharmaceuticals policy Supplementary protection certificate European Patent Organisation Patent European Patent Convention Summary of Product Characteristics
9	Application for paediatric extension of a Supplementary Protection Certificate for a Medicinal Product Please consult the Guide for filling in the Application for paediatric extension of a Supplementary Protection Certif Add to Reading List Source URL: iprights.dkpto.org Language: English - Date: 2016-05-17 05:23:18 Foreign relations Law Government Intellectual property law Patent law of the European Union Supplementary protection certificate Patent law Pharmaceutical industry Marketing authorization European Patent Convention Term of patent Patent application
10	Application for grant of a Supplementary Protection Certificate for Plant Protection Products Please consult the Guide for filling in the Application for grant of a Supplementary Protection Certificate for Plant Protecti Add to Reading List Source URL: iprights.dkpto.org Language: English Law Foreign relations Government Intellectual property law Pharmaceutical industry Marketing authorization Pharmaceuticals policy European Patent Organisation Supplementary protection certificate Patent European Patent Convention Trademark

UPDATE