European Clinical Trial Registry

Transparency And Disclosure Of Clinical Trials And Results
Transparency and Disclosure of Clinical Trials and Results Angelika Joos Head Regulatory Policy, Pan African Clinical Trial Registry European Medical Research Councils / European Science Foundation ... Fetch Document

Lost To Follow-up - Wikipedia, The Free Encyclopedia
Patients who become lost to follow-up during a clinical research trial result in many negative effects on the outcome of the trial and "Find Patients Lost To Follow-Up for Improved Clinical Trial Results." Thurs 13 Medicine | European Journal of Heart Failure. Web. 4 May 2011. ... Read Article

Overview Of FDAAA And Other Trial Registration Policies
•European Union requires registration and results Revised NIH Definition of “Clinical Trial”: Overview of FDAAA and Other Trial Registration Policies Author: National Library of Medicine Subject: ... Access Full Source

Clinical Trial Registries Conference
Clinical Trial Registries Conference Speaker Mr David J. Cocker Clinical Trials Unit WHO Primary Registry DRKS Germany Speaker Mr Andrew Freeman R & D Policy Director European Medicines Agency European Union Programme Committee and Speaker ... Doc Viewer

Antiarrhythmic Drugs For Atrial Fibrillation - About.com Health
Six antiarrhythmic drugs are often used to treat atrial fibrillation: propafenone added to the fact that clinical trials have A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the European Society of ... Read Article

Clinical trials In Developing Countries Submitted To EMEA For ...
17 Clinical Trial database/registry and public information • EudraCT – database of clinical trials – All trials with at least one site in the EEA ... Access This Document

Patient Information And Informed Consent - TREAT-NMD
Patient Information and Informed Consent When a clinical trial is being planned, European registry, we will not transfer any of your personal details, and your records will only be identifiable by the code they have been assigned. ... Access This Document

What Is AAT Deficiency? - Definition - About.com Health
AAT deficiency, or Alpha-1-antitrypsin deficiency, American Thoracic Society/European Respiratory Society Statement: "Clinical Features and Natural History of Severe Alpha-1 Antitrypsin Deficiency". Chest 1997; 111: ... Read Article

A European Paediatric Clinical Trials Register.
A European Paediatric Clinical Trials Register. Sammons H, Conroy S, Choonara I, Pandolfini C, Bonati M, Jacqz-Aigrain E, Danes I, Fuenttes I, Arnau J. ... Access Doc

SUSAR Rev2-11 04 06 Final - European Commission
5.4 Reporting of safety issues following completion of the clinical trial in the European Community After termination of the clinical trial, any unexpected safety issue that changes the risks Microsoft Word - SUSAR Rev2-11 04 06 Final.doc ... Fetch Full Source

BMTA Clinical Trials Globalization Nov2008.ppt
European clinical data • European Union Clinical • Migration of clinical trials to India, Russia and China European Union Clinical Trial Directive (2001) WHO Clinical Trial Registry ... Access Doc

Curcumin - Wikipedia, The Free Encyclopedia
Curcumin (/ ˈ k ər k juː m ə n /) is Clinical studies in humans with high doses (2–12 grams) of curcumin have shown few side-effects, [4] with some subjects reporting mild nausea or diarrhea. [5] ... Read Article

United States National Library Of Medicine - Wikipedia, The ...
The United States National Library of Medicine (NLM), operated by the United States federal government, AIDSinfo.nih.gov A comprehensive resource providing HIV/AIDS treatment and clinical trial information; SIS (Specialized Information Services), ... Read Article

Disclosure Clinical Trials - Pfizer
Disclosure of Clinical Trials Information 2009 Beyond Registration to Posting of Results . Calls for increasing information about tria ls included several major initiatives in ... Doc Retrieval

Turbulence, Trials, And Toxic Torts - ACE Limited
Expands the clinical trial registry database (www. clinicaltrials.gov), creates a new clinical trial results agency.5 In the European Union, Ethics Committees are required under the Clinical Trials Directive.6 ... Fetch This Document

Clinical Observational Research On Alzheimer’s Disease: What ...
Clinical Observational Research on Alzheimer’s Disease: Chinese Clinical Trial Registry; Clinical Tri-als Registry – India; Clinical Research Information Multinational study supported by the European Union NCT01425957 C8) ... Doc Viewer

Vol. 8, No. 10, October 2012 Happy Trials To ... - First Clinical
Vol. 8, No. 10, October 2012 ―Happy Trials to You ‖ Subscribe free at www clinical trial protocols 2001 European Commission a comparison of registry reports, clinical study reports, and journal publications. BMJ 2012;344:d8141. ... View This Document

GUIDELINES FOR CONDUCTING CLINICAL TRIALS OF MEDICINES, FOOD ...
GUIDELINES FOR CONDUCTING CLINICAL TRIALS OF MEDICINES, FOOD SUPPLEMENTS, 3.1 Clinical Trial Application A proof of registration with a Clinical Trials Registry (approved by The Board) 3.1.6. Investigator’s Brochure (COA, GMP) ... Retrieve Content

Merck Perspective Clinical Trial Registries And The ...
Merck Perspective Clinical Trial Registries and the Publication of Clinical Trial Results THE ISSUE Merck conducts clinical trials worldwide to evaluate the safety and efficacy of our ... View Full Source

Dynamics Of Clinical Trial Studies
Dynamics of Clinical Trial Studies Dr. Bayya Subba Rao & Dr. P. V. Appaji (European Region) 91507 33.96 3 WPRO (Western Pacific Region) 51100 18.96 Number of Registrations at Indian Clinical Trial Registry-Indian states, other countries-as on 9th March, ... Retrieve Full Source

Frequently Asked Questions - Paul Ehrlich Institute
Frequently Asked Questions EU Clinical Trials Register URL: https://www.clinicaltrialsregister.eu/ What is the EU Clinical Trials Register? What does it do? ... Visit Document

Clinical Trial Data Sharing Policy - Celgene
POLICY Clinical Trial Data Sharing Policy 1 . 1. PURPOSE . This policy establishes the responsibilities of Celgene employees and contractors with respect to ... Fetch Full Source

[NAME OF NATIONAL REGULATORY AUTHORITY] PROCEDURE FOR SUBMISSION
2of 19 General Procedures for clinical trial applications for vaccines and Biologicals Guidelines for the Review & Evaluation Process of Applications for ... Return Doc

What Is A registry? What Is A Biobank? - YouTube
What is a registry? What is a biobank? Thursday, Sharing Clinical Trial Data: Maximizing Benefits, Minimizing Risk - Duration: 59:06. Genetic Alliance 207 views. Cancer Registries & Clinical Trials - Duration: 1:06:00. ... View Video

Clinical Trial Transparency - PhUSE Wiki
Clinical Trial Transparency 14 March 2015 Pooja Phogat (No Registry Available) Clinicaltrials.gov implemented FDAMA 113 (Mar 2002) Registry Available European Clinical Trial Database (EudraCT) EudraCT, https://www.clinicaltrialsregister.eu ... Read Document