BUSINESS CONSULTING AND MANAGEMENT IN THE FIELD OF CLINICAL TRIALS, NAMELY, PRE-CLINICAL THROUGH PHASE FOUR CLINICAL RESEARCH AND CLINICAL TRIAL MANAGEMENT SERVICES, NAMELY, PRE-STUDY DOCUMENT COLLECTION AND REVIEW, SITE SELECTION, VISITS AND AUDITS, SITE COMPLIANCE, PROJECT TRACKING AND MONITORING REPORTS, NEGOTIATION AND ADMINISTRATION OF INVESTIGATOR GRANTS AND CLINICAL TRIAL BUDGETS AND CONTRACTS, FINANCIAL AND MANAGEMENT ACCOUNTING, DISTRIBUTION, COORDINATION AND TRACKING OF CLINICAL TRIAL PRODUCTS AND MATERIALS, REGULATORY DOCUMENT PROCESSING, LABORATORY SELECTION AND COORDINATION; BUSINESS CONSULTING AND MANAGEMENT IN THE FIELD OF CLINICAL TRIALS, NAMELY, PRE-CLINICAL THROUGH PHASE FOUR CLINICAL TRIAL MANAGEMENT SERVICES, NAMELY, MANAGING SITE AND STUDY-SPECIFIC SUBJECT RECRUITMENT STRATEGIES AND PROGRAMS IN THE NATURE OF CONTINGENCY STRATEGIES AND SOLUTIONS TO ADDRESS SPECIFIC PROJECT CHALLENGES; BUSINESS CONSULTING AND MANAGEMENT IN THE FIELD OF CLINICAL TRIALS, NAMELY, PRE-CLINICAL THROUGH PHASE FOUR CLINICAL TRIAL MANAGEMENT SERVICES, NAMELY, MANAGING THE DEVELOPMENT OF ALL STUDY RELATED DOCUMENTS AND MATERIALS IN THE NATURE OF STUDY PROTOCOLS, CONTRACTS, BUDGETS, AMENDMENTS, PAPER AND ELECTRONIC CASE REPORT FORMS, INFORMED CONSENT FORMS, SAFETY NARRATIVES, PRESENTATION POSTERS, AND TRAINING MANUALS; BUSINESS CONSULTING AND MANAGEMENT IN THE FIELD OF CLINICAL TRIALS, NAMELY, PRE-CLINICAL THROUGH PHASE FOUR CLINICAL TRIAL MANAGEMENT SERVICES, NAMELY, MANAGING ALL ASPECTS OF STUDY, DRUG RECONCILIATION, AND INVENTORY AND DISTRIBUTION REPORTS, MANAGING ALL ASPECTS OF CLINICAL TRIALS, NAMELY, MANAGING INVESTIGATORS, COORDINATORS, MONITORS, TECHNICIANS, AND PARTICIPANTS, ETHICAL REVIEWS, INVESTIGATOR MEETINGS, DATABASES, STATISTICAL ANALYSES AND REPORTING, RANDOMIZATION LOGISTICS, RECRUITMENT OF INVESTIGATORS, COORDINATORS, MONITORS, TECHNICIANS AND PARTICIPANTS; BUSINESS CONSULTING AND MANAGEMENT IN THE FIELD OF CLINICAL TRIALS, NAMELY, PHASE ONE THROUGH PHASE FOUR ADMINISTRATION OF CLINICAL TRIAL MANAGEMENT SERVICES, NAMELY, THE ADMINISTRATION OF PROTOCOLS INVOLVING VOLUNTEER RESEARCH PATIENTS AND THE RECRUITING OF SUCH VOLUNTEER RESEARCH PATIENTS; PROVIDING DATA MANAGEMENT SERVICES IN THE MEDICAL, PHARMACEUTICAL AND BIOTECHNOLOGICAL FIELD

PROVIDING TRAINING IN THE FIELD OF CLINICAL TRIALS AND CLINICAL TRIAL MANAGEMENT FOR THE PHARMACEUTICAL AND BIOTECHNOLOGICAL INDUSTRIES

MEDICAL AND SCIENTIFIC RESEARCH CONSULTING REGARDING PRECLINICAL TO PHASE FOUR CLINICAL TRIALS; PROVIDING QUALITY ASSURANCE SERVICES IN THE PHARMACEUTICAL AND BIOTECHNOLOGICAL INDUSTRIES

REGULATORY AFFAIRS, NAMELY, REVIEWING STANDARDS AND PRACTICES TO ASSURE COMPLIANCE WITH CLINICAL TRIAL LAWS AND REGULATIONS