BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Criterion Edge - ECPv6.18.3//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:Criterion Edge
X-ORIGINAL-URL:https://criterionedge.com
X-WR-CALDESC:Events for Criterion Edge
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:America/Los_Angeles
BEGIN:DAYLIGHT
TZOFFSETFROM:-0800
TZOFFSETTO:-0700
TZNAME:PDT
DTSTART:20250309T100000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0700
TZOFFSETTO:-0800
TZNAME:PST
DTSTART:20251102T090000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:-0800
TZOFFSETTO:-0700
TZNAME:PDT
DTSTART:20260308T100000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0700
TZOFFSETTO:-0800
TZNAME:PST
DTSTART:20261101T090000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:-0800
TZOFFSETTO:-0700
TZNAME:PDT
DTSTART:20270314T100000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0700
TZOFFSETTO:-0800
TZNAME:PST
DTSTART:20271107T090000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=America/Los_Angeles:20260923T080000
DTEND;TZID=America/Los_Angeles:20260923T090000
DTSTAMP:20261028T184230Z
CREATED:20260923T141200Z
LAST-MODIFIED:20261028T184230Z
UID:11387-1790150400-1790154000@criterionedge.com
SUMMARY:Turn Scientific Information into Organization-Wide Insights with AI
DESCRIPTION:As scientific literature continues to grow\, traditional systematic literature reviews (SLRs) can leave valuable insights siloed in individual reports. AI-powered evidence intelligence can help life sciences teams make scientific evidence more accessible\, reusable\, and actionable across the organization. \nIn this webinar\, our experts explore how pharmaceutical and medical device companies can combine AI\, systematic literature review methodology\, and human scientific expertise to improve evidence management\, support regulatory readiness\, and reduce duplicated effort. \n\nMove Beyond One-Time Literature Reviews\nLearn how continuous literature monitoring can help teams identify emerging evidence\, risks\, gaps\, competitor activity\, and changes in the state of the art.\nUnderstand Where AI Fits in the SLR Process\nExplore how AI can support literature discovery\, screening\, categorization\, and summarization—while experienced scientists provide the interpretation and regulatory context needed to maintain rigor.\nCreate a Shared Evidence Foundation Across Teams\nDiscover how structured\, reusable evidence can support Regulatory Affairs\, Medical Affairs\, R&D\, and Clinical teams while improving consistency and efficiency.\n\nWatch Now
URL:https://criterionedge.com/event/turn-scientific-information-into-organization-wide-insights-with-ai/
LOCATION:Webinar\, United States
CATEGORIES:Pharma Webinars
ATTACH;FMTTYPE=image/webp:https://criterionedge.com/wp-content/uploads/Turn-Scientific-Information-into-Organization-Wide-Insights-with-AI-scaled.webp
ORGANIZER;CN="Criterion Edge":MAILTO:support@criterionedge.com
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Los_Angeles:20261028T080000
DTEND;TZID=America/Los_Angeles:20261028T090000
DTSTAMP:20261028T185441Z
CREATED:20261028T183219Z
LAST-MODIFIED:20261028T185441Z
UID:12147-1793174400-1793178000@criterionedge.com
SUMMARY:Beyond AI: Why the Future of Scientific and Regulatory Writing Is Human + AI
DESCRIPTION:AI is becoming increasingly common in scientific and regulatory writing\, but using it effectively requires more than simply automating existing workflows. In regulated environments\, teams must balance AI-driven efficiency with scientific judgment\, evidence traceability\, quality control\, and human accountability. \nIn this webinar\, Criterion Edge explores a human + AI approach to scientific and regulatory writing\, including where AI can improve efficiency\, where it introduces risk\, and how teams can integrate AI without compromising regulatory rigor. \n\nUnderstand Where AI Adds Value—and Where It Falls Short\nExplore how AI can assist with literature screening\, data extraction\, drafting\, and error detection\, as well as common risks such as hallucinated citations\, missing evidence\, and incorrect clinical context.\nMaintain Regulatory Rigor and Evidence Traceability\nLearn why AI-assisted regulatory writing still requires documented methodologies\, reproducible evidence trails\, expert verification\, and human accountability throughout the workflow.\nBuild a Practical Human + AI Workflow\nDiscover how to introduce AI strategically\, validate outputs\, strengthen QC processes\, and use scientific experts for the higher-level interpretation and decision-making AI cannot replace.\n\nWatch Now
URL:https://criterionedge.com/event/beyond-ai-why-the-future-of-scientific-and-regulatory-writing-is-human-ai/
LOCATION:Webinar\, United States
CATEGORIES:IVDR Webinars,MDR Webinars,Pharma Webinars
ATTACH;FMTTYPE=image/jpeg:https://criterionedge.com/wp-content/uploads/zoom-webinar-graphic-261028.jpg
ORGANIZER;CN="Criterion Edge":MAILTO:support@criterionedge.com
END:VEVENT
END:VCALENDAR