Expert Insights Webinars
Award-winning experts share their detailed and actionable insights to inform
the future of pharma and biotech.
EU CTR Compliance and Success: Navigating Updates and Preparing Submissions for the EU CTIS Portal
As of January 31, 2023, Sponsors are required to submit all new trial applications for authorization in the European Union through the Clinical Trial Information System (CTIS) in compliance with the new European Union Clinical Trials Regulation (EU CTR).
In this webinar, a cross-functional team, including clinical trial transparency specialists and medical writers, will share best practices and insights to help Sponsors better prepare their submissions for the EU CTIS portal.
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How to Create Fit-For-Purpose Clinical Study Reports for Successful Submissions
Using Natural Language Processing (NLP) to curate unstructured EHR
Strategies for Navigating ICH E9(R1)
Insights and Trends from 2021 FDA GCP Inspections.
Tips for Effective and Efficient New Drug Application (NDA) Submissions
Strategies for Rare Disease Data Analysis: Doing More with Less
Orphan Drug, Rare Pediatric Disease and Expedited Program Designations
Rare Disease Research in the United States, Part 2
Rare Disease Research in the United States, Part 1
The Blueprint for Success for Effective and Efficient Clinical Protocols
EU Clinical Trials Regulation: The Clinical Trial Transparency Revolution
Avoiding Common Pitfalls in the IND and CTA Submission Process
Evolving Your FSP Relationships to Achieve Maximum Return
How to Use Machine Learning in Clinical Research Right Now