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How do we “do” consent? Clinical & research models in Genomic Medicine

August 12 2020 @ 2:00 PM - 3:00 PM

Clinical & research models in Genomic Medicine

HOW DO WE ‘DO’ CONSENT? CLINICAL & RESEARCH MODELS IN GENOMIC MEDICINE: 100,000 GENOMES PROJECT AND BEYOND

 

In this webinar, Prof Christine Patch will talk through what has been achieved in the “patient choice” process of consent developed during 100k Genomes and reflect on the challenges of creating an ethically robust research ecosystem as a routine part of clinical care.

Find the webinar link and further details on the Wellcome Genome Campus event page.

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Details

Date:
August 12 2020
Time:
2:00 PM - 3:00 PM
Event Categories:
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Event Tags:
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Website:
https://societyandethicsresearch.wellcomegenomecampus.org/catalogue/how-do-we-do-consent-clinical-research-models-in-genomic-medicine-100000-genomes-project

Venue

Online
United Kingdom

Organiser

Wellcome Genome Campus Advanced Courses and Scientific Conferences
Website:
https://coursesandconferences.wellcomegenomecampus.org/

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With any Whole Genome Sequencing (WGS) test ordered, a Record of Discussion (RoD) form will also need to be submitted. This document is to record the patient’s consent for genomic testing and their choice on taking part in research. Guidance on the patient choice conversation can be found here. 
 
This RoD form will be available for clinicians to download from this webpage. Once completed with the patient, it can be send to the lab with the corresponding test order form and sample.
Tests available to order will be listed in the National Genomic Test Directory. A test order form will soon be made available for clinicians on this webpage to download and complete. This form will include the address of the laboratory that the appropriate sample and completed form needs to be sent to.
 
Until the new Genomic Laboratory Service goes live, please continue to follow existing test order processes.
 
Later this year, the online test ordering tool for Whole Genome Sequencing will be integrated into the National Genomics Informatics System (NGIS) and clinicians will be able to search or filter to find a clinical indication, confirm eligibility criteria and start the test request process for their patient.