The core business of Mediprobe Research is the conduct of Phase II-IV national and international clinical trials in the field of dermatology.

Mediprobe works with pharmaceutical companies to develop study designs and write study protocols, case report forms and written informed consent forms.

We conduct Phase II-IV clinical trials to GCP standards and meet all applicable regulatory requirements.


  • Study design, protocol/information consent preparation, case report form and database development
  • Regulatory submission for initial and ongoing approval to a central IRB, (REB), Health Canada (TPD), FDA
  • Clinical trial coordinators with in-house phlebotomy/ processing and shipping of blood samples
  • Experienced data management group to produce reports/manuscripts/other medical literature

Call us at 519-657-4222 ext. 250