MEDICEMENT RESEARCH SERVICES

Site and PI Identification• Site Development• System & SOP Designing• Complete Site Management starting from Site Identification, Site Selection,Training, Site Initiation, Enrolment, Follow-up, Monitoring, Audit, Data Management to Site Clouse-out• Co-ordination with Sponsor, CRO, Central Clinical Laboratory, Core Laboratory, Ethics Committee, Other Logistic Partners • All Clinical Research Documentation• IP Management Services• Site Supply & Logistic Management• Good Clinical Practices (GCP) Training• Medicine Information Services• Teaching & Training the Students & Healthcare Professionals• Adverse Event Analysis & Pharmacovigilance• Hospital / Clinics Patient's Data Compilation • Data Mining & Epidemiology Research• Research Project Design• Protocol Design• Informed Consent, Case Report Form designing• Clinical Data Collection• Clinical Data compilation• Clinical Research Variable Analysis• Statistical Analysis• Journal Article Writing