<--- Back to Details
First PageDocument Content
Scientific method / Institutional review board / Good Clinical Practice / Clinical Trials Directive / Clinical trial / Declaration of Helsinki / Ethics Committee / Regulatory requirement / Informed consent / Clinical research / Research / Science
Date: 2012-08-07 10:48:20
Scientific method
Institutional review board
Good Clinical Practice
Clinical Trials Directive
Clinical trial
Declaration of Helsinki
Ethics Committee
Regulatory requirement
Informed consent
Clinical research
Research
Science

Add to Reading List

Source URL: www.unicri.it

Download Document from Source Website

File Size: 257,11 KB

Share Document on Facebook

Similar Documents

Stellungnahme der Bundesärztekammer zum Konsultationspapier der Europäischen Kommission vomzur “Clinical Trials Directive” EC

DocID: 1s7cN - View Document

Medical research / Clinical research / Research / Medical ethics / Clinical research ethics / Pharmaceuticals policy / Design of experiments / Clinical Trials Directive / Ethics committee / Clinical trial / Institutional review board / Informed consent

Comments of the German Medical Association To the Consultation Paper of the European Commission ofon the ‘Clinical Trials Directive’ EC

DocID: 1rjyu - View Document

Medical research / Medicine / Research / European Union directives / Clinical research / Research ethics / Medical technology / Medical device / Ethics committee / Clinical Trials Directive / Medical Devices Directive / Medical ethics

Response of the German Medical Association to the proposal by the European Commission for a Regulation of the European Parliament and of the Council on medical devices, and amending DirectiveEC,

DocID: 1rdN0 - View Document

Medical research / Clinical research / Health / Multi-speed Europe / Clinical data management / EudraCT / Clinical pharmacology / European Economic Area / Clinical Trials Directive / Clinical trial / Supplementary protection certificate

Trial results: Modalities and timing of posting VersionAprilInterventional Clinical Trials that ended on or after 21 Julyi.e. the date of finalisation of the programming according to Commission Gui

DocID: 1r4sk - View Document

Medical research / Health / Clinical research / Pharmaceutical industry / Agencies of the European Union / Drug discovery / Pharmaceuticals policy / European Medicines Agency / Heads of Medicines Agencies / Clinical trial / Good clinical practice / Clinical Trials Directive

Reflection Paper on ethical and GCP aspects of clinical trials

DocID: 1r4bZ - View Document