Webinars>>Clinical Study
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How to Create an Electronic Informed Consent
Are you uncertain about the essential elements your form should contain to meet legal requirements and ensure every subject's safety and willing participation? Our exclusive seminar on "How to Create an Electronic Informed Consent" is designed just for you! Why should I attend: In this webinar, we ensure to cover following essential key components that must be part of an electronic informed consent. 1. Personal Information: Collecting important details like name, address, email, date of birth, and relevant medical history ensures a clear record of the participant's identity and background. 2. Purpose of the Study or Research: Participants need to know why they're being asked to take part. We'll teach you how to convey the purpose of your study or research effectively. 3. Procedure or Event Details: Set clear expectations for your participants by detailing what they can expect during the trial or event, including its duration and possible termination conditions. 4. Voluntary Participation Assurance: Participants must be informed that their involvement is entirely voluntary, and they have the right to withdraw at any stage without consequences. 5. Risk Disclosure: Transparency is key. We'll guide you in listing potential risks or inconveniences alongside potential positive outcomes, ensuring participants make well-informed decisions. 6. Reimbursements and Costs: Make sure your form clearly states any reimbursements or financial costs involved, along with compensation or treatment options in case of any adverse events. 7. Confidentiality Statement: If applicable, your form should address who can access participants' information and the measures taken to protect their privacy. 8. Additional Legal Information: Depending on your industry and form's purpose, we'll help you include any other mandatory information to ensure compliance. Not only will we cover the essential elements, but we'll also equip you with best practices to create user-friendly, efficient, and concise consent forms. Remember, your participants' experience matters most! Our seminar ensures your content is crystal clear, includes all mandatory elements, and remains user-friendly throughout. Sign up today and unlock the power of informed consent. Who will benefit:
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For additional information on this webinar topic, please call 410-501-5777 or email: info@fdamap.com
