Clinical Trial Services in Nashik

SponsorCRO Clinical Project Management CRF Design Data management Design of Clinical Trial Logs ICF Design Independent Audit Pharmacovigilance Monitoring & Outsourcing Preparation of Investigator's Brochure Protocol Development Site Feasibility and Selection Site Identification Translation And Back Translation of ICF   InvestigatorSite Final Study Report Development GCP training to Investigator and site staff Institutional Ethics Committee Negotiation of site contractbudget Providing study coordinators (CRCs) Site initiation and close out activities Site Management And Study Supply Subject Recruitment support