№ lp_1_2_31015
Guidance on structure, language, and presentation of informed consent forms for healthy adult participants in interventional clinical trials involving a trial medicine.
Document type: Guidance document
Subject: Informed consent in interventional clinical trials
Population: Healthy adult participants
Scope: Interventional clinical trials with trial medicine
Jurisdiction: Belgium
Organizations mentioned: CT College; Healixia; Ethics Committees; Belgian Data Protection Authority
Language versions: English; French; Dutch
Intended users: Clinical trial sponsors
Regulatory context: Ethics Committee submission requirements
Version: 1.0
Price: 8 / 10 USD
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