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Clinical Trials Directive
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1	Stellungnahme der Bundesärztekammer zum Konsultationspapier der Europäischen Kommission vomzur “Clinical Trials Directive” EC Add to Reading List Source URL: www.bundesaerztekammer.de - Date: 2014-10-01 03:07:02
2	Comments of the German Medical Association To the Consultation Paper of the European Commission ofon the ‘Clinical Trials Directive’ EC Add to Reading List Source URL: www.bundesaerztekammer.de Language: English - Date: 2014-10-01 03:07:02 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
3	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, Add to Reading List Source URL: www.bundesaerztekammer.de Language: English - Date: 2014-10-01 03:09:29 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
4	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 Add to Reading List Source URL: www.clinicaltrialsregister.eu Language: English - Date: 2016-07-13 04:51:15 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
5	Reflection Paper on ethical and GCP aspects of clinical trials Add to Reading List Source URL: www.fercap-sidcer.org Language: English - Date: 2012-05-16 01:59:10 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
6	The Agency for Medicinal Products and Medical Devices of the Republic of Slovenia has prepared the unofficial consolidated text for the Medicinal Products Act which includes:  Medicinal Products Act (Official Gazette Add to Reading List Source URL: www.jazmp.si Language: English - Date: 2013-07-12 06:13:47 Pharmaceuticals policy Health Medical research Clinical Trials Directive Directive 2001/83/EC Good laboratory practice Marketing authorization Good Clinical Practice Directive European Pharmacopoeia Biopharmaceutical Pharmacovigilance European Medicines Agency
7	PDF Document Add to Reading List Source URL: www.efpia.eu Language: English - Date: 2016-04-04 06:14:49 Medical research Health Clinical trials Clinical research Pharmaceuticals policy Drug discovery Pharmaceutical industry Pharmacovigilance European Federation of Pharmaceutical Industries and Associations ClinicalTrials.gov European Medicines Agency Clinical Trials Directive
8	Government Response to the House of Commons Science and Technology Committee Inquiry into Clinical Trials Cm 8743 Add to Reading List Source URL: www.gov.uk Language: English - Date: 2013-11-18 09:12:23 Medical research National Health Service Clinical research Health Research Pharmaceutical industry Clinical pharmacology National Institute for Health Research Clinical trial AllTrials NHS Constitution for England Clinical Trials Directive
9	EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE-GENERAL Consumer goods Pharmaceuticals Brussels, Add to Reading List Source URL: sfbct.free.fr Language: English - Date: 2013-09-12 15:12:41 Medical research Pharmaceuticals policy Clinical research Pharmaceutical industry European Union directives European Union Clinical Trials Directive Good Clinical Practice Directive Clinical trial EudraLex Good clinical practice Traceability
10	REFLECTION PAPER -‐ EFPIA Guiding Principles on Layperson Summary EU Clinical Trials Regulation – Annex V Add to Reading List Source URL: www.efpia.eu Language: English - Date: 2016-04-05 10:42:36 Medical research Clinical research Clinical trials Clinical trial ClinicalTrials.gov European Federation of Pharmaceutical Industries and Associations Clinical trial portal Clinical Trials Directive