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 Government Authorities for investigational new drugs, preparing statistical reports resulting from clinical trials

Training clinical trial site personnel concerning drug protocol requirements and the use of tests and rating system for such protocol; training clinical trial site personnel in the use of medical and research equipment required by drug protocols