Trial Participants: Informed Consent, GCP, Patient Involvement
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1. Who Contributes to the Running of a Clinical Trial?
(This section is organised in the form of a book, please follow the blue arrows to navigate through the book or by following the navigation panel on the right side of the page.)
- Research institutes.
- Patient organisations.
- Pharmaceutical companies.
- Governments.
- Universities.
- The trial design.
- Scientific and ethical review procedures.
- Deciding which participants should be included in the trial.
- Finding and recruiting the appropriate participants.
- Guarantee full protection of participants taking part in the clinical trial.
- And more…