CRB Workshop: Clinical Research Methodology & Management

This workshop has been developed to provide overview of clinical research process with a comprehensive review of ICH GCP, Site Management,Ethical concerns, USFDA, Schedule Y and the elements involved in coordinating Clinical Research.

Who should attend?

  • Participants having affiliation to hospitals, medical, pharmacy etc.
  • Biotechnology institutions contract research organizations
  • Site management organizations, independent clinical research firms
  • Pharmaceutics and biotechnology companies
  • Clinical research education & training centres
  • Clinical research investigators
  • Clinical research coordinators
  • Clinical research associates
  • Clinical research project managers
  • Clinical research administrators
  • Clinical research consultants
  • Clinical research educators
  • Clinical research students
  • Post graduate students in Medicine, Pharmacology
  • Pharmacy and life sciences looking for a career in clinical research