{"665377":{"#nid":"665377","#data":{"type":"event","title":"Bench2Market Talks","body":[{"value":"\u003Cp\u003E\u003Cem\u003E\u003Cstrong\u003E\u0026quot;Medical Device and IVD Regulatory Overview\u0026quot;\u003C\/strong\u003E\u003C\/em\u003E\u003C\/p\u003E\r\n\r\n\u003Cp\u003E\u003Cstrong\u003E\u003Ca href=\u0022https:\/\/www.linkedin.com\/in\/sandra-d-maher-30a293a\/\u0022\u003ESandra D. Maher. M.S.\u003C\/a\u003E\u003Cbr \/\u003E\r\nIndependent Regulatory Affairs Consultant\u003C\/strong\u003E\u003Cbr \/\u003E\r\n\u0026nbsp;\u003C\/p\u003E\r\n\r\n\u003Cp\u003E\u003Cstrong\u003ETo attend virtually via Zoom, \u003Ca href=\u0022https:\/\/gatech.zoom.us\/webinar\/register\/WN_OAnKKzoLShqej1aB8QJCEQ\u0022\u003Eregister HERE\u003C\/a\u003E.\u003C\/strong\u003E\u003C\/p\u003E\r\n\r\n\u003Cp\u003EHave you ever wondered what it takes to take a medical technology through the FDA?\u0026nbsp;Join us for a discussion on Medical Devices and an IVD Regulatory Overview to\u0026nbsp;help you better understand some of the considerations for determining a product\u0026#39;s regulatory route to market.\u0026nbsp;This introduction is for professionals new to medical device and IVD regulatory affairs and looking for an opportunity to learn more about regulatory requirements for bringing products to market.\u003C\/p\u003E\r\n\r\n\u003Cp\u003E\u003Ca href=\u0022https:\/\/gatech.us12.list-manage.com\/track\/click?u=0303937b37f9138ed964fb8f4\u0026amp;id=edbf25aded\u0026amp;e=c1c3e45f20\u0022 target=\u0022_blank\u0022 title=\u0022https:\/\/gatech.us12.list-manage.com\/track\/click?u=0303937b37f9138ed964fb8f4\u0026amp;id=edbf25aded\u0026amp;e=c1c3e45f20\u0022\u003ESandra D. Maher, M.S.\u003C\/a\u003E, Regulatory Affairs Consultant (Medical Devices and IVDs), will cover topics including defining a medical device and an IVD, reviewing basics about device classification, identifying different types of premarket submissions, and describing how to get a new product to market.\u0026nbsp;\u003C\/p\u003E\r\n\r\n\u003Cp\u003E\u003Cem\u003EThis event is the 5th session in the 2022-2023 Bench2Market Talks series, which was created to provide commercialization guidance to the university research community.\u003C\/em\u003E\u003C\/p\u003E\r\n","summary":null,"format":"limited_html"}],"field_subtitle":"","field_summary":"","field_summary_sentence":[{"value":"\u0022Medical Device and IVD Regulatory Overview\u0022 - Sandra D. Maher, M.S., Regulatory Affairs Consultant "}],"uid":"35486","created_gmt":"2023-02-01 21:22:38","changed_gmt":"2023-02-01 21:23:11","author":"Christina Wessels","boilerplate_text":"","field_publication":"","field_article_url":"","field_event_time":{"event_time_start":"2023-02-15T11:30:00-05:00","event_time_end":"2023-02-15T13:00:00-05:00","event_time_end_last":"2023-02-15T13:00:00-05:00","gmt_time_start":"2023-02-15 16:30:00","gmt_time_end":"2023-02-15 18:00:00","gmt_time_end_last":"2023-02-15 18:00:00","rrule":null,"timezone":"America\/New_York"},"extras":[],"groups":[{"id":"638977","name":"Biolocity"},{"id":"655285","name":"GT Commercialization"},{"id":"1292","name":"Parker H. Petit Institute for Bioengineering and Bioscience (IBB)"},{"id":"1254","name":"Wallace H. Coulter Dept. of Biomedical Engineering"}],"categories":[],"keywords":[{"id":"187423","name":"go-bio"},{"id":"188880","name":"go-bio-commercialization"},{"id":"189814","name":"go-researchevents"}],"core_research_areas":[],"news_room_topics":[],"event_categories":[{"id":"1795","name":"Seminar\/Lecture\/Colloquium"}],"invited_audience":[{"id":"78761","name":"Faculty\/Staff"},{"id":"177814","name":"Postdoc"},{"id":"78771","name":"Public"},{"id":"174045","name":"Graduate students"},{"id":"78751","name":"Undergraduate students"}],"affiliations":[],"classification":[],"areas_of_expertise":[],"news_and_recent_appearances":[],"phone":[],"contact":[],"email":[],"slides":[],"orientation":[],"userdata":""}}}