Documents
On this page you can find all our documents in English, including our Glossary and Guide to Biobanks in Sweden. Documents published on this website are administrated and updated by Biobank Sweden and may not be changed. Biobank Sweden guarantees the content only if the original version is used.
For questions or feedback regarding the documents, please contact info@biobanksverige.se
Information and forms for the public
General Information
Forms for access to samples
L1. Access to sample collection and personal data for research
L1a. Appendix Information about existing clinical samples in pathology and cytology biobanks
L1b. Appendix: Information about existing samples in biobanks
L1f. Regions included in the study
L1g. Appendix. Samples in study
N2. Request for alteration of agreement according to the multicentre principle
N4. Signing of power of attorney
N3a. Report on completed study sampling in multicentre studies
N3b. Appendix 1, Report on completed sampling
T1. Access to biobank samples and sample code in clinical trials
Instructions and checklists
K4. Instruction for completion of form L1
K1c. Appendix_Checklist for Researcher who is Sample Collection Controller
M1. Multicentre principle instruction
M2a. Overview of the multicenter principle
Ti1. Anvisning yttrande enligt EU-förordningar kliniska prövning
Ti4. Handledning sponsor – process vid ansökan om klinisk prövning
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About Biobank Sweden
Biobank Sweden is a national infrastructure for biobanking where healthcare, academia, industry and patient organisations collaborate to attain good healthcare and research.
BIOBANK SVERIGE • C/O REGIONALT BIOBANKSCENTRUM MELLANSVERIGE • AKADEMISKA SJUKHUSET • 751 85 UPPSALA