Biobank Sweden is not a biobank but a national infrastructure for biobanking where healthcare, academia, industry, and patient organisations collaborate to attain good healthcare and research.
Here on our website you can find information and documents regarding how to access samples in Swedish biobanks for research, method development or clinical trials.
The guide “Sample handling in national studies” is now available for download. The guide contains a schematic overview of important steps for studies wishing to collect biobank samples from multiple locations around Sweden. Biobank Sweden’s Sample Service Coordinators have well-established networks and are familiar with the procedures and services, as well as sample and data […]
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After careful considerations, Biobank Sweden’s steering group has decided to remove the form N3. The document has previously been used to report on completed sampling in multi centre studies. It has emerged that these reports constitute an obstacle for both researchers and sponsors, as well as for Regional Biobank Centres (RBCs) and E-biobank managers, who […]
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Biobank Sweden has secured project funding through Swelife to ensure a continued development of the successful model ‘healthcare integrated biobanking’. The project which will go on until 2026, aims to increase the efficiency of the national model and thereby strengthening medical research while also contributing to equal care and health benefits in Sweden. Healthcare integrated […]
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In these interviews, reseachers share their personal reflections on how biobanks aid research and the development of improved healthcare.
Here you can see our upcoming webinars, conferences, courses and more!
1 September 2025
Online
This webinar introduces the Precision Omics Initiative Sweden (PROMISE), which aims to expand biobank resources, integrate genomic data into healthcare, and establish a sustainable framework for precision medicine research. Save the date!
1 September 2025
Online
9 September 2025
Online
A talk by Lara Bloom. Lara Bloom is the President and CEO of The Ehlers-Danlos Society and responsible for globally raising awareness of rare, chronic, and invisible diseases, specializing in the Ehlers-Danlos syndromes (EDS), hypermobility spectrum disorders (HSD), and related conditions. Lara leads coordinated medical collaboration, raising funds for research and focuses on global progression, […]
9 September 2025
Online
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