[The GCP directive--consequences for clinical drug research]. [electronic resource]
Producer: 20030603Description: 1662-4 p. digitalISSN:- 0041-5782
- Adverse Drug Reaction Reporting Systems -- legislation & jurisprudence
- Clinical Trials as Topic -- legislation & jurisprudence
- Clinical Trials, Phase IV as Topic -- legislation & jurisprudence
- Denmark
- Drug Approval -- legislation & jurisprudence
- Drug Monitoring -- standards
- European Union
- Guidelines as Topic
- Humans
- Practice Guidelines as Topic
- Quality Assurance, Health Care
- Research Design -- legislation & jurisprudence
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Publication Type: English Abstract; Journal Article
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