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Volumn 48, Issue 2, 2005, Pages 141-146
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Harmonisation of regulatory requirements for clinical trials on medicinal products for human use in the Directive 2001/20/EC and complementary guidance. Implementation of the 12th Law Amending the German Drug Law;Angleichung der regulatorischen Anforderungen für die klinische Prüfung von Arzneimitteln am Menschen in der EU. Die Richtlinie 2001/20/EG und die diese ergänzenden Verordnungen und Empfehlungen: Die 12. Novelle zum AMG
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Author keywords
Clinical trial; Directive 2001 20 EC; German drug law; Medicinal product
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Indexed keywords
DRUG;
ADVISORY COMMITTEE;
ARTICLE;
CLINICAL RESEARCH;
CLINICAL STUDY;
DRUG LEGISLATION;
DRUG RESEARCH;
DRUG USE;
EUROPEAN UNION;
GERMANY;
GOOD CLINICAL PRACTICE;
GOVERNMENT REGULATION;
HUMAN;
LEGAL ASPECT;
PATIENT RIGHT;
PRACTICE GUIDELINE;
PROFESSIONAL STANDARD;
RESEARCH ETHICS;
ADULT;
ADVERSE DRUG REACTION REPORTING SYSTEMS;
CHILD;
CLINICAL TRIALS;
EUROPE;
EUROPEAN UNION;
GERMANY;
GUIDELINE ADHERENCE;
HUMANS;
INFORMED CONSENT;
INTERNATIONAL COOPERATION;
LEGISLATION, DRUG;
MINORS;
QUALITY ASSURANCE, HEALTH CARE;
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EID: 14844345959
PISSN: 14369990
EISSN: None
Source Type: Journal
DOI: 10.1007/s00103-004-0978-1 Document Type: Article |
Times cited : (2)
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References (12)
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