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Should You Become A Clinical Investigator?
Will You Expose Your Practice to Legal Liabilities?
Who Gets the Grants?
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additional adverse events amended at 52 audit blood pressure Budget under control CenterWatch clinical hold clinical investigation clinical research clinical studies clinical trials Collection of information conduct consent form contract contract research organization control number Data and information Declaration of Helsinki described disease Drug Administration drug application enrollment Evaluation and Research Food and Drug ical individual information requirements approved informed consent initial Institutional Review Board inves investigational drug investigational new drug investigator's June 17 life-threatening Management and Budget marketing application meeting monitor novice investigator number of patients obtain Office of Management organizations paragraph pharmaceutical companies phase III trials physician potential practice procedures protocol amendment records recruit regulations report forms request responsible risks side effects site's SMOs specific sponsoring company sponsors and CROs study coordinator submission submitted test article therapeutic therapy tigator tion treatment IND treatment protocol volunteers