Informed Consent

Chicken Soup Series - Informed Consent

(Mar 2023) How to obtain informed consent from subjects with cognitive impairment
(Nov 2022) Regulatory Guidance on Consent Requirements for Clinical Trials involving Collection and Use of Human Tissue
(Apr 2022) Changes to Assent requirements and Documentation - How does it impact your study?
(Feb 2022) Informed Consent Process During Covid-19 Period
(Oct 2021) When is Re-Consenting of Research Subjects Needed?
(Aug 2021) Impartial Witness & Witness in Informed Consent-Taking for HBR Studies
(Dec 2020) Pointers for Electronic Consent (e-Consent)
(Nov 2020) Informed Consent: When is an Impartial Witness Needed?
(Nov 2019) How should Consent be obtained from Subjects Lacking Mental Capacity?
(May 2019) Witness requirements for Informed Consent process
(Oct 2018) Obtaining Consent for Adults lacking mental capacity in Human Biomedical Research
(Jul 2018) Re-consenting for HBR studies extending past 31 October 2018 involving the use of individually identifiable data/ materials
(Apr 2018) Processes for Consenting a Subject into a Clinical Trial in an Emergency Situation
(Sep 2017) How should Consent be obtained for Subjects who are unable to read?

_DISCLAIMER_{: Past Issues/Articles may contain best practices, policies or SOPs that have been superseded or may no longer relevant or applicable. For NHG and partner institutions, we encourage you to refer to the latest NHG PCR SOPs (available via NHG Intranet access or Partner Institution’s CRU/Research office). Always refer to your own institution’s latest policy, SOPs, guidance documents and templates.}