
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.
Services:
- 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