EXPERIENCE THE EXCEPTIONAL

PMR Highlights

  • Over 60 clinical research facilities in USA, Canada, Australia,
    and Chile
  • Experience in Phase I, II, III, and IV clinical trials
  • Investigators have conducted more than 1,300 unique clinical trials
  • Over 32,000 patients followed in those trials
  • Consistently the top enrolling sites
  • Responsible for driving the subject recruitment timelines in
    many studies resulting in earlier submissions to regulatory
    authorities
  • High quality data as evidenced by 56 regulatory inspections (FDA, Health
    Canada, & EMEA)
  • Key opinion leaders (KOL) who have consulted on compound
    development for over 270 pharmaceutical companies
  • Contribute to and guide protocol development for realistic and feasible
    studies
  • Present clinical data due to vast experience with products that are
    developed
  • Authorship

Pharmaceutical, CRO, or Clinic?

Get in touch with us! Fill out this form to get in contact with a member of the PMR team. We’d love to explore partnering with you!





    By pressing the "Send" button, you confirm that you give the company your consents for processing your personal data.