WCT

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

BUILDING INSPECTION, NAMELY, INSPECTING POTENTIAL SITES FOR HOSTING CLINICAL TRIALS

TRAINING CLINICAL TRIAL SITE PERSONNEL CONCERNING DRUG PROTOCOL REQUIREMENTS AND THE USE OF TESTS AND RATING SYSTEMS FOR SUCH PROTOCOL; TRAINING CLINICAL TRIAL SITE PERSONNEL IN THE USE OF MEDICAL AND RESEARCH EQUIPMENT REQUIRED BY DRUG PROTOCOLS

TECHNICAL WRITING OF CLINICAL REPORT FORMS WHICH ARE REQUIRED BY CLINICAL TRIAL DRUG PROTOCOLS; TECHNICAL WRITING OF CLINICAL TRIAL REPORTS; DATABASE DEVELOPMENT SERVICES TO PROCESS DATA COLLECTED FROM CLINICAL TRIALS