Advisory services and training

Are you planning a research project, need guidance on quality registries or registry data, or simply want to discuss a question?
UCR provides methodological support, training and advisory services in clinical research and quality registries. Our expertise includes study design, project management, monitoring, biostatistics, data management and tools for data collection, from idea to analysis and publication.

UCR supports all stages of the research process, where robust study design, appropriate methods and quality assurance are essential for reliable results.
We encourage you to contact us early in your planning, for example when preparing a funding application.

Our team has broad expertise and experience in:

  • biostatistics, quality registries and the conduct of clinical studies
  • collaboration with academia, industry and healthcare
  • national and international studies
  • regulatory processes and dialogue with authorities
  • planning data collection and ensuring data quality, including data flow design and selection of data capture tools
  • information security and data protection
  • quality assurance in line with regulations for clinical trials of medicinal products and medical devices

Quality assurance

Support in ensuring quality and compliance with regulations, such as GCP and ISO 14155.

Information security and data protection

Support in ensuring compliance with data protection regulations, including GDPR.

Education and training


UCR offers training courses and seminars tailored to different needs and target groups.

In addition to regularly scheduled courses, we also offer customised training based on your requirements.

Contact

  • Phone UCR: 018-611 00 00 (UCR)
    Telephone exchange: 018-611 00 00
    (Akademiska sjukhuset)
    E-mail: info@ucr.uu.se

Visit us

Uppsala Clinical Research Center
Uppsala Science Park, Hubben
Dag Hammarskjölds väg 38
751 85 Uppsala

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