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Registries and biobanks: Background, obstacles, and practical views

Studies that include large patient data registries are an example of more complex observational studies, and the same is true for studies that use extensive biobanks. This session will provide information on what you need to know when working on such projects, and will furthermore provide plenty of practical examples, including hurdles and pitfalls. After a short presentation, there will be plenty of time for questions from you as researchers.

This seminar session is part of a lunch seminar series, which offers brief overviews and room for questions on important topics related to observational studies (HRO projects). Find out more about the whole seminar series here: Facts and pitfalls for observational studies - How to plan and conduct HRO projects

About this session

This seminar session gives insights about common pitfalls when working with large sets of clinical patient data and biological samples. We will look at practical tips for planning projects and research questions, up to regulatory requirements and real-life examples.

Content and speakers:

Specificities for projects with registries and biobanks:

Background and what you need to know:

  • What are registries/biobanks?
  • Project planning and approval process
  • Regulatory requirements for registry projects
  • Common pitfalls

Insights from the practice:

  • Learnings from an international registry
  • Practical tips and real-life examples

Speakers:

  • Claudia Becherer (Teamleader Regulatory Affairs, Department of Clinical Research, Basel)
  • Sina Hansen, PhD (Scientific Officer Coordination & Project Management, Department of Clinical Research, Basel)
Who should attend:

Researchers with planned, ongoing, or completed HRO projects (observational studies), who are working with data registries or biobanks.

When:

Wednesday, 8 May 2024, 12h00 – 13h00

Presentations / Video

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