Bioavailability/Bioequivalence Studies

  • Study Design for Full BA/BE Studies
  • Protocol Preparation
  • Case Report Form Design
  • Subject Recruitment For Healthy Volunteers or Required Special Population
  • Administration of Drug/Drug Products to Subjects and Sampling Blood/Urine

Clinical Trials

  • Phase I
  • Phase IIA
  • Phase IIB
  • Phase III
  • Late Phase clinical Trials
  • Post Marketing Surveillance