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PRODID:-//Eurobiomed - ECPv6.10.3//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:Eurobiomed
X-ORIGINAL-URL:https://www.eurobiomed.org
X-WR-CALDESC:Évènements pour Eurobiomed
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:Europe/Paris
BEGIN:DAYLIGHT
TZOFFSETFROM:+0100
TZOFFSETTO:+0200
TZNAME:CEST
DTSTART:20250330T010000
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BEGIN:STANDARD
TZOFFSETFROM:+0200
TZOFFSETTO:+0100
TZNAME:CET
DTSTART:20251026T010000
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BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20251126T100000
DTEND;TZID=Europe/Paris:20251126T113000
DTSTAMP:20260405T023758
CREATED:20251107T162102Z
LAST-MODIFIED:20251107T162444Z
UID:30955-1764151200-1764156600@www.eurobiomed.org
SUMMARY:European Medicines Agency: Regulatory Support Tools for Innovative Medicines & Technologies Developers
DESCRIPTION:The Council of European Bioregions (CEBR) is a European network bringing together around 50 health clusters\, including Eurobiomed. \nFor this exclusive webinar\, CEBR is partnering with the European Medicines Agency (EMA) to present the regulatory support tools available to developers of innovative medicines and health technologies. \nJoin us to hear directly from the EMA\, gain first-hand insights into their support mechanisms\, and ask your questions live to their experts. \nYou’ll hear from two key speakers from the EMA who will share their expertise and insights: \n\nHélène Casaert – Scientific Officer\, EMA\n\nHélène is a Scientific Officer within the SME Office\, where she provides dedicated support to small and medium-sized enterprises developing medicines in the EU and fosters innovation across the sector. \nBefore joining the EMA\, she worked as a Regulatory Affairs Manager in the pharmaceutical industry and in the clinical trials division of the French national competent authority. \n\nSebastian Asprella – Programme Lead\, EMA\n\nSebastian leads EU competitiveness initiatives at the EMA\, focusing on predictable\, science-based regulatory pathways that help clusters\, tech transfer offices\, and SMEs translate European scientific excellence into tangible patient benefits. \n 
URL:https://www.eurobiomed.org/evenement/european-medicines-agency-regulatory-support-tools-for-innovative-medicines-technologies-developers/
LOCATION:Webinaire\, Webinaire
CATEGORIES:Évènement expert
ATTACH;FMTTYPE=image/png:https://www.eurobiomed.org/wp-content/uploads/2025/11/Visuel-CEBR-x-EMA.png
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