Clinical

Drugs, Natural Health Products, Medical Devices 

Clinical Trial Applications (CTA)

Investigational Device Exemptions (IDE)

Clinical Trial Master File (TMF)

Clinical Trial Registration with US ClinicalTrials.gov

Institutional / Ethics Review Board (IRB / ERB) Consulting

Study Design Review & Strategy

Investigator Brochure (IB)

Informed Consent Declaration

Case Report Forms (CRF)

Study Reports

Study Product Labeling 

Medical Writing

Investigational Drug Safety Reporting 

Good Clinical Practice (GCP) Audit