{"id":45714,"date":"2022-02-14T11:47:52","date_gmt":"2022-02-14T16:47:52","guid":{"rendered":"https:\/\/www.arisglobal.com\/?p=45714"},"modified":"2022-02-14T11:47:52","modified_gmt":"2022-02-14T16:47:52","slug":"arisglobal-presents-idmp-for-global-regulatory-affairs-at-dia-rsidm","status":"publish","type":"post","link":"https:\/\/www.arisglobal.com\/media\/press-release\/arisglobal-presents-idmp-for-global-regulatory-affairs-at-dia-rsidm\/","title":{"rendered":"ArisGlobal Presents IDMP for Global Regulatory Affairs at DIA RSIDM"},"content":{"rendered":"

LifeSphere product leaders share insight into how an effective IDMP strategy can support various business functions<\/strong><\/h3>\n

MIAMI, FL and VIRTUAL, February 14, 2021 – ArisGlobal, the leading provider of life sciences software that automates core drug development functions with its end-to-end technology platform LifeSphere\u00ae, today announced two of its product leaders from its Regulatory segment will be presenting an on demand session at the 2022 DIA Regulatory Submissions, Information, and Document Management Forum (RSIDM) virtual and in person event.<\/p>\n

Event details:<\/p>\n

Session Title: Beyond Regulatory Information Management: Leveraging IDMP Across All Business Functions to Proactively Manage Global Regulatory Affairs<\/p>\n

Session Date\/Time: On Demand, Monday, February 14 \u2013 Wednesday, February 16, 2022<\/p>\n

Speakers:
Sonia Hurley, Sr. Director, Product Management, Regulatory
Robin Schilling, IDMP Product Manager<\/p>\n

Sonia Hurley, Sr. Director, Product Management, Regulatory, is a seasoned regulatory professional with over 20 years of experience with highly regulated products in the Biotech\/Life Sciences arena.<\/p>\n

Robin Schilling<\/a>, IDMP Product Manager, brings a diverse portfolio of 20 years of experience across government, military intelligence and life sciences. She is the product lead supporting the development and updates to LifeSphere IDMP.<\/p>\n

LifeSphere IDMP has been recognized by industry analysts Gens & Associates as the most-ready IDMP<\/a> software available.<\/p>\n

At DIA\u2019s Regulatory Submissions, Information, and Document Management (RSIDM) Forum, attendees will hear from industry and regulatory stakeholders working across the scope of regulatory information to examine current and evolving data standards and requirements and effective regulatory information management approaches to align related systems.<\/p>\n","protected":false},"excerpt":{"rendered":"

LifeSphere product leaders share insight into how an effective IDMP […]<\/p>\n","protected":false},"author":27,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[65],"tags":[],"class_list":["post-45714","post","type-post","status-publish","format-standard","hentry","category-press-release"],"acf":[],"yoast_head":"\nArisGlobal Presents IDMP for Global Regulatory Affairs at DIA RSIDM | ArisGlobal<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.arisglobal.com\/media\/press-release\/arisglobal-presents-idmp-for-global-regulatory-affairs-at-dia-rsidm\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"ArisGlobal Presents IDMP for Global Regulatory Affairs at DIA RSIDM\" 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