Frequently Asked Questions About Electronic and Remote Consent

Remote consent (sometimes referred to as “teleconsent”) is a method of obtaining informed consent using a paper or electronic consent form where the study team ...

Use of Electronic Informed Consent: Questions and Answers

In general, OHRP and FDA guidance documents do not establish legally enforceable responsibilities. Instead, guidances describe the current ...

remote-consent-and-e-consent29aug2022v3.docx

BSPH IRB Frequently Asked Questions about Remote Consent and Electronic Consent (e-consent) ... consent form (or remote paper consent) is a ...

eIC Frequently Asked Questions

Can eIC be used for all research projects? ... Yes, electronic consent can be used for full board and expedited protocols to facilitate remote consent or ...

Use of Electronic Informed Consent in Clinical Investigations - FDA

Use of Electronic Informed Consent in Clinical Investigations – Questions and Answers Guidance for Institutional Review Boards, Investigators, ...

eConsent Frequently Asked Questions - Vibrent Health

eConsent, short for electronic consent, refers to the process of obtaining and documenting informed consent from individuals electronically.

4 questions to ask about electronic informed consent - MassDevice

4 questions to ask about electronic informed consent · New_IMARC_LOGO What is electronic informed consent? · How do we ensure the electronic ...

E-Consent: Benefits, Challenges, and Considerations

○ General concerns about online security. ○ Confidentiality of ... Use of Electronic Informed Consent Questions and Answers. Published ...

Electronic Information Systems (EIS) Policy: Frequently Asked ...

A: For technical questions or assistance regarding an electronic system, please contact your ... Electronic Informed Consent (eIC). X.

ORARC Tip Sheet: REMOTE INFORMED CONSENT

and then discuss it and ask any questions together with the investigator. 3 ... FDA-regulated research that employs an electronic informed consent (eIC) process.

Remote Consent - Office for Human Subject Protection

Study teams often assume that 'remote consent' equates to electronic consent ... ask questions to the study team about the research prior to providing consent.

Q: Electronic methods for consent in research - Capella FAQs

When consent is required, researchers who decide to obtain consent via a remote method (a method that is not face-to-face) should keep in ...

Informed Consent FAQs - HHS.gov

Yes, under certain circumstances. First, the investigator and the IRB need to be aware of relevant laws pertaining to electronic signatures in the jurisdiction ...

Informed Consent Guidance Now Available - NRG Oncology

... your institution is in compliance with the requirements for remote consent. ... All research personnel may find the “Frequently asked Questions ...

Informed Consent: An IRB Perspective on Navigating the New Normal

From a regulatory standpoint, remote consent is permissible as long as consent is documented. ... Answers to frequently asked questions related to research and ...

FDA: Use of Electronic Informed Consent Q&A - Validation Center

FDA Guidance: Use of Electronic Informed Consent Questions and Answers, 12/16 · Are understandable and easy for users to navigate · Retain all versions of IC ...

E-consent guidance FINAL 06 11 21 (1).pdf - Columbia | Research

Electronic Consent (e-Consent): the use of electronic systems and processes, whether in person or remotely, that employ electronic media (e.g., ...

Top 4 eConsent Questions in Clinical Research - Castor EDC

Question 1: How does eConsent align with the traditional consent process? ... In brief, eConsent is the electronic version of informed consent.

Remote Consent Procedures: Revised FAQs due to COVID-19

The purpose of Remote Consent is to allow the investigator/designee and potential participant to engage in the informed consent process in a way ...

Frequently Asked Questions about Remote Consent - CDN

Electronic consent. If you have given your consent to join the study using the electronic consent form you do not need to send a copy to your ...