Beschreibung
Webinar: Clinical Trials – The Data Science Perspective (12.09.2025)
Basis Webinar, 12.09.2025
Beginn: 10:00 Uhr
Ende: ca. 11:30 Uhr
Themengebiet: GCP
What exactly happens in a clinical trial?
This webinar offers a behind-the-scenes look at the clinical research process – from the initial study design to data collection and data analysis. You will learn who is involved, what their responsibilities are, and where data professionals play a crucial role.
In the second part, we will focus on the regulatoriy landscape that shapes clinical research and data science. You’ll get an overview of essential international guidelines such as ICH GCP R3, FDA regulations, and the Act on Artificial Intelligence, as well as current AI policies in healthcare. Understanding these frameworks is key for anyone working with data in a clinical setting.
Stay Ahead in Clinical Research with Data Science
This webinar is your entry point into one of the most dynamic intersections in modern healthcare: data science and clinical research.
Additional Module
- From Data to Insight – Data Management and Analysis in Clinical Trials
Book both modules an save 15 %
Key Topics at a Glance
- How clinical trials work: Sponsor, Investigator, and CRO roles
- Regulatory guidelines and compliance:
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- ICH GCP R3 (Good Clinical Practice)
- FDA regulations relevant to clinical data
- AI governance in healthcare: Act on AI & emerging AI policies
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Who Should Attend?
- Aspiring or early-career Data Scientists, Statisticians, and Programmers
- Professionals exploring a transition into clinical research or pharmaceutical development
- Specialists working in or with pharma companies, biotech firms, or CROs
Relevant industries
- Clinical Research & Development
- Pharmaceuticals & Biotechnology
Webinar: Clinical Trials – The Data Science Perspective (12.09.2025)
