Serious adverse event

Results: 260



#Item
1Microsoft Word - SOP editedonlineversibaru.doc

Microsoft Word - SOP editedonlineversibaru.doc

Add to Reading List

Source URL: www.ummc.edu.my

Language: English - Date: 2015-06-03 21:28:52
2Microsoft Word - Abbreviations List Approved Oct 2014

Microsoft Word - Abbreviations List Approved Oct 2014

Add to Reading List

Source URL: www.acrpnet.org

Language: English - Date: 2015-02-18 16:59:26
3Statement German Network for Evidence-based Medicine Berlin, 05 JulyThe German Network for Evidence-based Medicine endorses the

Statement German Network for Evidence-based Medicine Berlin, 05 JulyThe German Network for Evidence-based Medicine endorses the

Add to Reading List

Source URL: www.ebm-netzwerk.de

Language: English - Date: 2016-07-11 07:26:44
4Microsoft Word - Unanticipated_Problems

Microsoft Word - Unanticipated_Problems

Add to Reading List

Source URL: www.firstclinical.com

Language: English - Date: 2014-09-14 03:12:34
5PHARMACOVIGILANCE GUIDE FOR ADVERSE DRUG REACTION MONITORING AND CAUSALITY ASSESSMENT, 2015  Post marketing Control Division,

PHARMACOVIGILANCE GUIDE FOR ADVERSE DRUG REACTION MONITORING AND CAUSALITY ASSESSMENT, 2015 Post marketing Control Division,

Add to Reading List

Source URL: dra.gov.bt

Language: English - Date: 2016-07-27 06:22:23
6QuarterWatch Monitoring FDA MedWatch Reports Why Reports of Serious Adverse Drug Events Continue to Grow October 3, 2012 Data from 2012 Quarter 1

QuarterWatch Monitoring FDA MedWatch Reports Why Reports of Serious Adverse Drug Events Continue to Grow October 3, 2012 Data from 2012 Quarter 1

Add to Reading List

Source URL: www.ismp.org

Language: English - Date: 2012-10-03 12:53:27
7Improving Patient Care Better Reporting of Harms in Randomized Trials: An Extension of the CONSORT Statement John P.A. Ioannidis, MD; Stephen J.W. Evans, MSc; Peter C. Gøtzsche, MD, DrMedSci; Robert T. O’Neill, PhD; D

Improving Patient Care Better Reporting of Harms in Randomized Trials: An Extension of the CONSORT Statement John P.A. Ioannidis, MD; Stephen J.W. Evans, MSc; Peter C. Gøtzsche, MD, DrMedSci; Robert T. O’Neill, PhD; D

Add to Reading List

Source URL: www.consort-statement.org

Language: English - Date: 2013-08-14 20:08:36
8Minimum Criteria for ICH E6 GCP Investigator Site Personnel Training (Excerpt from TransCelerate BioPharma Operating Principles) Scope The intent of this document is to define the Minimum Criteria for Good Clinical Pract

Minimum Criteria for ICH E6 GCP Investigator Site Personnel Training (Excerpt from TransCelerate BioPharma Operating Principles) Scope The intent of this document is to define the Minimum Criteria for Good Clinical Pract

Add to Reading List

Source URL: www.transceleratebiopharmainc.com

Language: English - Date: 2015-12-07 16:54:46
9Pharmaceutics / Science / Design of experiments / Pharmacology / Clinical trial / Serious adverse event / Adverse event / Institutional review board / Regulatory requirement / Clinical research / Pharmaceutical industry / Research

DOC Document

Add to Reading List

Source URL: globalhealthtrials.tghn.org

Language: English - Date: 2012-06-06 06:50:59
10PREOPANC SERIOUS ADVERSE EVENT FORM Septform 10

PREOPANC SERIOUS ADVERSE EVENT FORM Septform 10

Add to Reading List

Source URL: www.pancreaskanker.nl

Language: English - Date: 2014-10-14 11:19:39