EudraCT

Results: 165



#Item
131Pharmaceutical sciences / European Medicines Agency / EudraCT / Clinical trial / EudraVigilance / Clinical Trials Directive / Regulatory requirement / Pharmacovigilance / European Forum for Good Clinical Practice / Clinical research / Research / Health

Mandate for the HMA Clinical Trials Facilitation Group (CTFG) Background and introduction Following the implementation of the Clinical Trials Directive[removed]EC in May 2004 the EU Heads of Medicines Agencies establish

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Source URL: www.hma.eu

Language: English - Date: 2012-02-08 09:06:03
132Science / Evaluation methods / Nursing research / Clinical Data Management / EudraCT / ClinicalTrials.gov / Clinical trial / Comment / Clinical research / Research / Pharmaceutical industry

Form for submission of comments

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:33:01
133Pharmaceutical sciences / Health / Pharmacology / Pharmaceutical industry / European Union / European Medicines Agency / Clinical Trials Directive / EudraLex / EudraCT / Clinical research / Research / Pharmaceuticals policy

Communication from the Commission — Detailed guidance on the request to the competent authorities for authorisation of a clinical trial on a medicinal product for human use, the notification of substantial amendments a

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:00:38
134Pharmaceuticals policy / Quality assurance / Audit / Qualified Person / Health / Science / Learning / Clinical research / Clinical Data Management / EudraCT

Association Européenne des Spécialités Pharmaceutiques Grand Public Association of the European Self-Medication Industry Europäischer Verband der Arzneimittel-Hersteller AESGP comments on the Template for the Qualifi

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:30:25
135Health / Science / Pharmaceutical industry / Clinical Data Management / EudraCT / Drug discovery / Clinical trial / Servier / Clinical research / Research / Medical statistics

Page 1 of 1 FUEHRING Stefan (SANCO) From: [removed]

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:32:50
136Design of experiments / Pharmacology / Scientific method / Pharmaceutical industry / Clinical trial / Drug discovery / Institutional review board / EudraCT / Clinical research / Research / Science

Declaration of the End of Trial Form (cf

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 08:59:10
137Science / Clinical Data Management / Food and Drug Administration / Pharmacology / EudraCT / Clinical trials registry / Clinical trial / Validation / ClinicalTrials.gov / Clinical research / Research / Pharmaceutical industry

SUBMISSION OF COMMENTS ON <GUIDELINE TITLE> <DOCUMENT REFERENCE>

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:32:53
138Pharmaceutical sciences / Pharmacology / Clinical Data Management / EudraCT / Clinical trials / ClinicalTrials.gov / Clinical trials registry / Clinical trial / Pharmacovigilance / Clinical research / Research / Pharmaceutical industry

Association of Clinical Research Organizations Comments in Response to the European Commission Public Consultation on the “Implementing Technical Guidance- List of Fields for Result-Related Information to be Submitted

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:32:48
139Pharmaceutical industry / Health / Pharmaceutical sciences / Clinical Data Management / EudraCT / Qualified Person / EudraGMP / European Medicines Agency / Audit / Clinical research / Pharmaceuticals policy / Research

Submission of comments on TEMPLATE FOR THE QUALIFIED PERSON’S DECLARATION CONCERNING GMP COMPLIANCE OF INVESTIGATIONAL MEDICINAL PRODUCTS MANUFACTURED IN NON-EU COUNTRIES

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:30:25
140Health / Clinical Data Management / EudraCT / Clinical trials / National Institutes of Health / ClinicalTrials.gov / EudraPharm / Clinical trials registry / Database / Clinical research / Research / Pharmaceutical industry

Implementing technical guidance – List of fields for result-related information to be submitted to the ‘EudraCT’ clinical tria

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:32:49
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