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REGULATION on clinical trials of medicinal products in humans, No[removed], as amended by Regulations No[removed]and No[removed]
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Document Date: 2013-05-10 11:14:42

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Company

Agency for the Evaluation / /

Country

Iceland / /

IndustryTerm

pharmaceutical form / clinical trial protocol / investigational medicinal product / foreign pharmaceutical authorities / investigational medicinal products / satisfactory insurance coverage / pharmaceutical production / trial medicinal products / trial protocol / medicinal product / trial product / biological product / comparable medicinal products / manufacturing / manufacturing practice / chemical / clinical pharmaceutical study / advertising value / control / medicinal products / trial medicinal product / medicinal product manufacturer / /

MedicalCondition

same illness / congenital defect / injury / illness / /

MedicalTreatment

gene therapy / cell therapy / /

Organization

European Agency for the Evaluation of Medicinal Products / International Medical Association / National Bioethics Committee / Icelandic Medicines Agency / Personal Data Protection Authority / /

Position

Investigator / Supervisor / trial supervisor / dentist / Principal investigator / head physician / physician / principal investigator / cf. item f. f / investigators and principal investigator / investigator/principal investigator / auditor / representative / director of the ward / General / /

ProgrammingLanguage

EC / /

Technology

gene therapy / cell therapy / same clinical trial protocol / clinical trial protocol / trial protocol / 27 Protocol / 9 Trial protocol / /

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