Serious adverse event - PDFSEARCH.IO - Document Search Engine

Serious adverse event
Results: 260

#	Item
241	Form for submission of comments Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:32:48 Pharmaceutical sciences Research Pharmaceutical industry Adverse effect Serious adverse event Clinical Trials Directive Pharmacovigilance Clinical trial Adverse event Clinical research Pharmacology Health
242	Public consultation on re-written guidance on SUSAR (suspected unexpected serious adverse reaction) reporting during Clinical Trials September 2010 Cancer Research UK welcomes the opportunity to comment on the re-written Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:32:48 Medicine Health Pharmacology Drug safety Design of experiments Clinical trial Serious adverse event Adverse event Clinical Trials Directive Clinical research Research Pharmaceutical industry
243	Communication from the Commission — Detailed guidance on the collection, verification and presentation of adverse event/reaction reports arising from clinical trials on medicinal products for human use (CT-3) Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:00:40 Pharmaceutical sciences Health Pharmacology Pharmaceuticals policy Drug safety Serious adverse event Adverse event Clinical Trials Directive Pharmacovigilance Clinical research Research Pharmaceutical industry
244	Ref. Ares[removed][removed]EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – quality, safety and efficacy Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:00:44 Pharmaceutics Science EudraCT Clinical trial Clinical Trials Directive Adverse event Serious adverse event Clinical research Research Pharmaceutical industry
245	Item / Section number Comment Item 41 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:02 Pharmacology Pharmaceutical sciences Science Drug safety Design of experiments Serious adverse event Clinical trial Pharmacovigilance Adverse event Clinical research Research Pharmaceutical industry
246	Page 1 of 2 FUEHRING Stefan (SANCO) From: MERJ (Merete Jørgensen) [[removed]] Sent: jeudi 30 septembre[removed]:18 To: SANCO PHARMACEUTICALS Cc: LBWR (Lill-Brith von Arx); MERS (Merete Schmiegelow); VBJE (Vibe Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:32:48 Pharmaceutics Science ClinicalTrials.gov EudraCT Novo Nordisk Clinical trial European Federation of Pharmaceutical Industries and Associations Serious adverse event Adverse event Clinical research Pharmaceutical industry Research
247	Joint Research Compliance Office This is a controlled document. The master document is posted on the JRCO website and any print-off of this document will be classed as uncontrolled. Add to Reading List Source URL: workspace.imperial.ac.uk Language: English - Date: 2013-07-08 06:36:01 Pharmaceutical sciences Health Pharmacology Serious adverse event Adverse effect Adverse event Medicines and Healthcare products Regulatory Agency Clinical trial Pharmacovigilance Clinical research Research Pharmaceutical industry
248	EUROPEAN COMMISSION Brussels, [removed]SWD[removed]final VOLUME II (Annexes) Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:29:42 Clinical Trials Directive EudraLex Clinical trial Good Clinical Practice Pharmacovigilance EudraCT Ethics Committee Medical research Serious adverse event Clinical research Research Health
249	Microsoft Word - vol_9b_2011-10.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:59:17 Clinical research Medicine Pharmaceuticals policy Drug safety Pharmaceutical industry Pharmacovigilance EudraVigilance European Medicines Agency Serious adverse event Pharmaceutical sciences Pharmacology Health
250	KPO SOLUTIONS Overview To streamline our processes we have set up a Knowledge Process Outsourcing Add to Reading List Source URL: www.medhimalayas.com Language: English - Date: 2009-10-13 01:47:50 Health Clinical research Pharmaceutical industry Drug safety Pharmacy Pharmacovigilance Adverse event Serious adverse event Medical device Pharmacology Medicine Pharmaceutical sciences

UPDATE