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DTSTAMP:20260901T134555Z
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SUMMARY:How do you design a clinical study that is registration-ready?
DESCRIPTION:A study that is suitable for publication or guideline development is not automatically suitable for marketing authorisation. Hellen Houlleberghs\, Orfenix’ s clinical director will discuss what changes when the goal is registration of a product instead of just a publication. She will discuss what changes including: study design and endpoints\, study preparation\, CTIS readiness\, GCP\, IMP logistics\, common pitfalls\, timelines\, and post-study obligations. \nParticipants will also receive the “From protocol to registration readiness scan”\, a practical tool to identify potential gaps in their own study. \nVisit the website for more information: https://orfenix.com/webinar-how-do-you-design-a-clinical-study-that-is-registration-ready/ \n Registration link: https://events.teams.microsoft.com/event/b00fe972-6382-435a-8b8c-19b6abf772f0@5b8666c1-d3a4-4d81-841c-691b9585ca11
URL:https://remedi4all.org/event/how-do-you-design-a-clinical-study-that-is-registration-ready/
LOCATION:Webinar
ATTACH;FMTTYPE=image/png:https://remedi4all.org/wp-content/uploads/2026/09/Or_webinar-2-hellen-clinical-featured-image-980x551-1.png
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