This program will benefit individuals involved in:

  • Clinical Research and Development
  • Clinical Safety and Pharmacovigilance
  • Clinical Trial and Project Management
  • Data Management
  • Drug Development and Discovery
  • Investigator Site Management
  • Medical and Scientific Affairs
  • Academia
  • Outsourcing Management
  • Contract Research Organizations
  • Post-graduate Students Entering Pharmaceutical Industry
  • Procurement and Purchasing
  • Quality Assurance
  • Regulatory Affairs
  • Government and Public Policy; Lawmakers
  • Senior and Executive-Level Decision Making for Clinical Trial
  • All Stakeholders and Vendors of CR Industry