PMR Highlights

  • Over 70 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
  • 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

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