Clinical trials Frequently Asked Questions
- Outline of the Process
- Filing of Clinical Trials
- Adverse Drug Reaction Reporting
- Completion of Clinical Trials
- Clinical Trial Sites
- Qualified Investigator
- Research Ethics Board Attestation
- Drug Submission Application Form (HC/SC 3011)
- Drug Master Files (DMFs) in Support of CTAs Involving Pharmaceutical Drugs
- Drug Importation
- Record Keeping