CTIS Video Tutorial – Submitting Initial Clinical Trial Application in CTIS: Form & MSC Sections
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CTIS Video Tutorial – Submitting Initial Clinical Trial Application in CTIS: Part I (Sponsor)
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CTIS Video Tutorial - How to create, cancel or clear, and submit an annual safety report
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CTIS–M08 How to submit the final decision on the clinical trial application in the CTIS (Authority)
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CTIS – M08 How to assess an initial clinical trial application in CTIS – Part II
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CTIS - M14 How to submit, update and revert a Corrective Measure (Authority)
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CTIS Video Tutorial – Managing a Clinical Trial in CTIS: Trial & Recruitment Notices (Sponsor)
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CTIS - M16 How to create an inspection record and how to populate the General information section
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The Clinical Trial Information System (CTIS) is mandatory for all new clinical trials conducted in the EU. Navigate the complexities of CTIS and unlock its full potential! Access the following 3 webinars from our CTIS Master Series: - Webinar 1: Are you Ready for CTIS? - Webinar 2: Preparing Content for CTIS & the EU CTR - Webinar 3: Beyond First Impressions - Lessons Learned in the First 3 Months | Citeline
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CTIS - M15 How to view and download CTs in the authority workspace
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CTIS - M17 How to update and complete an ad hoc assessment
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Transition Your Clinical Trials to CTIS
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CTIS Bitesize Talk: Initial clinical trial application - March 2022
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CTIS - M06 How to access an initial CTA in CTIS – Validation - RFI and issue validation decision
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Clinical Trials in the EU
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CTIS Video Tutorial - How to search for a clinical trial in the CTIS sponsor workspace
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