35
Business management assistance and consultation for clinical trials of investigational drugs, namely, arranging for sites to perform clinical trials, arranging for the import, packaging, shipping, labeling, and distribution of drugs and other investigational supplies to and from the clinical trial sites, arranging for the central collection of laboratory specimens from clinical trial sites, making any and all filings required by the food and drug administration for investigational new drugs, preparing statistical reports resulting from clinical trials
42
Technical writing of clinical report forms for others which are required by clinical trial drug protocols; technical writing of clinical trial reports for others; database development services to process data collected from clinical trials
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