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DTSTART;TZID=America/New_York:20210727T110000
DTEND;TZID=America/New_York:20210727T150000
DTSTAMP:20240822T152600Z
CREATED:20210622T011148Z
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UID:10000226-1627383600-1627398000@swhr.org
SUMMARY:Noninvasive Prenatal Screening: Eliminating Barriers to Access and Reducing Disparities
DESCRIPTION:July 27\, 11 a.m.- 3 p.m. — Noninvasive Prenatal Screening (Day 1) \nJuly 30\, 11 a.m.-3 p.m. —Noninvasive Prenatal Screening Policy Discussion (Day 2) \nGenetic screening is a prime example of translating advances in human genomics research into an intervention with a direct benefit to public health. A variety of methods are available to screen adults\, fetuses\, and newborns — all with a goal of gaining insight into the risk posed by certain heritable conditions. \nNoninvasive prenatal screening (NIPS) can help women make informed decisions about their reproductive health and pregnancy management\, as well as improve maternal and fetal outcomes by allowing preparation to care for children who may be affected by a genetic disorder. However\, challenges with integrating research and development advances into health care and regulatory systems have left gaps in preventive care for patients. \nAs part of our Genetic Screening Program\, SWHR convened an interdisciplinary working group of health care providers\, medical professional society leaders\, patients/patient advocates\, policy experts\, and diagnostic company scientists for a closed roundtable meeting on July 27 and July 30 to discuss how to eliminate barriers to access and reduce health disparities related to NIPS.
URL:https://swhr.org/event/nips-roundtable-eliminating-barriers-to-access-and-reducing-disparities/2021-07-27/
LOCATION:Virtual Event
CATEGORIES:Policymaker Event,Roundtable,Science Event,SWHR Event
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DTSTART;TZID=America/New_York:20210729T110000
DTEND;TZID=America/New_York:20210730T150000
DTSTAMP:20240822T151652Z
CREATED:20210624T004648Z
LAST-MODIFIED:20240822T151652Z
UID:10000227-1627556400-1627657200@swhr.org
SUMMARY:Expanded Carrier Screening: Eliminating Barriers to Access and Reducing Disparities
DESCRIPTION:July 29\, 11 a.m.- 3 p.m. — Expanded Carrier Screening (Day 1) \nJuly 30\, 11 a.m.-3 p.m. — Expanded Carrier Screening Policy Discussion (Day 2) \nGenetic screening is a prime example of translating advances in human genomics research into an intervention with a direct benefit to public health. A variety of methods are available to screen adults\, fetuses\, and newborns — all with a goal of gaining insight into the risk posed by certain heritable conditions. \nExpanded carrier screening (ECS) can help women make informed decisions about their reproductive health and pregnancy management\, as well as improve maternal and fetal outcomes by allowing preparation to care for children who may be affected by a genetic disorder. However\, challenges with integrating research and development advances into health care and regulatory systems have left gaps in preventive care for patients. \nAs part of our Genetic Screening Program\, SWHR is convening an interdisciplinary working group of health care providers\, medical professional society leaders\, patients/patient advocates\, policy experts\, and diagnostic company scientists for a closed roundtable meeting on July 29-30 to discuss how to eliminate barriers to access and reduce health disparities related to ECS.
URL:https://swhr.org/event/ecs-roundtable-eliminating-barriers-to-access-and-reducing-disparities/
LOCATION:Virtual Event
CATEGORIES:Policymaker Event,Roundtable,Science Event,SWHR Event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20210730T080000
DTEND;TZID=America/New_York:20210730T170000
DTSTAMP:20240822T152600Z
CREATED:20210622T011148Z
LAST-MODIFIED:20240822T152600Z
UID:10000724-1627632000-1627664400@swhr.org
SUMMARY:Noninvasive Prenatal Screening: Eliminating Barriers to Access and Reducing Disparities
DESCRIPTION:July 27\, 11 a.m.- 3 p.m. — Noninvasive Prenatal Screening (Day 1) \nJuly 30\, 11 a.m.-3 p.m. —Noninvasive Prenatal Screening Policy Discussion (Day 2) \nGenetic screening is a prime example of translating advances in human genomics research into an intervention with a direct benefit to public health. A variety of methods are available to screen adults\, fetuses\, and newborns — all with a goal of gaining insight into the risk posed by certain heritable conditions. \nNoninvasive prenatal screening (NIPS) can help women make informed decisions about their reproductive health and pregnancy management\, as well as improve maternal and fetal outcomes by allowing preparation to care for children who may be affected by a genetic disorder. However\, challenges with integrating research and development advances into health care and regulatory systems have left gaps in preventive care for patients. \nAs part of our Genetic Screening Program\, SWHR convened an interdisciplinary working group of health care providers\, medical professional society leaders\, patients/patient advocates\, policy experts\, and diagnostic company scientists for a closed roundtable meeting on July 27 and July 30 to discuss how to eliminate barriers to access and reduce health disparities related to NIPS.
URL:https://swhr.org/event/nips-roundtable-eliminating-barriers-to-access-and-reducing-disparities/2021-07-30/
LOCATION:Virtual Event
CATEGORIES:Policymaker Event,Roundtable,Science Event,SWHR Event
END:VEVENT
END:VCALENDAR