Documents

On this page you can find all our documents in English. 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

For the public - Change of consent

pdf E1. Change of consent 10.2

For the public - Information

pdf G1. Samples taken within healthcare are stored – flyer, A4 10.2
pdf G1. Samples taken within healthcare are stored – flyer, A4 (for print) 10.2

All documents in English

pdf B1. Glossary 10.1
pdf E1. Change of consent 10.2
pdf G1. Samples taken within healthcare are stored – flyer, A4 10.2
pdf K2.1 Form Selector 10.0
pdf K4. Instructions for completing form L1.1, L1.2 and L1.3 10.2
pdf K5. Information on agreements when human biological material is to be sent for an action 10.0
docx L1.1. Application for establishment of sample collection for research 10.2
docx L1.2 Agreement on the release of samples and personal data 10.1
docx L1a. Appendix – Information about existing clinical samples in pathology and cytology biobanks 10.2
docx L1b. Appendix – Information about existing samples in biobanks 10.0
docx L2a1. AGREEMENT about making Human Biological Material available to a Research Principal for an Action 10.0
pdf L2a1a. Example of wording regarding the transfer of conditions in L2a1 10.0
docx L2a2. AGREEMENT about making Human Biological Material available for an Action in clinical trials and performance studies 10.0
docx L2a3. AGREEMENT about making Human Biological Material available when a Research Principal sends samples for an Action to a Recipient 10.0
docx N2. Request for amendment of agreement according to the multicentre principle 10.1
docx N3. Report on completed sampling in multicentre study 10.0
docx N4. Signing of power of attorney 10.0
docx T1.1. Establishment of sample collection for clinical trials and performance studies 10.1
docx T1.2. Agreement regarding release of samples for clinical trials and performance studies 10.1
docx T7a. Responsible biobank when newly collected samples are to be collected for clinical trials or performance studies 10.2
pdf Ti5.1 Instructions for completing form T1.1 and T1.3 10.1
pdf Ti6. Selection of form for clinical trials 10.0

Research - establishment and/or release of samples

docx L1.1. Application for establishment of sample collection for research 10.2
docx L1.2 Agreement on the release of samples and personal data 10.1
docx L1.3. Request for amendment of previously approved biobank application 10.0
docx L1a. Appendix – Information about existing clinical samples in pathology and cytology biobanks 10.2
docx L1b. Appendix – Information about existing samples in biobanks 10.0
docx L7. Responsible biobank for newly collected samples taken for research 10.3
pdf K4. Instructions for completing form L1.1, L1.2 and L1.3 10.2

Research - The multicentre principle

docx N2. Request for amendment of agreement according to the multicentre principle 10.1
docx N3. Report on completed sampling in multicentre study 10.0
docx N4. Signing of power of attorney 10.0

Research - Clinical trials/performance studies (CTR, MDR och IVDR)

docx T1.1. Establishment of sample collection for clinical trials and performance studies 10.1
docx T1.2. Agreement regarding release of samples for clinical trials and performance studies 10.1
docx T1.3 Request for amendment of biobank agreement for clinical trials and performance studies 10.0
docx T7a. Responsible biobank when newly collected samples are to be collected for clinical trials or performance studies 10.2
pdf Ti5.1 Instructions for completing form T1.1 and T1.3 10.1
pdf Ti6. Selection of form for clinical trials 10.0
docx N4. Signing of power of attorney 10.0
docx L1a. Appendix – Information about existing clinical samples in pathology and cytology biobanks 10.2

Research - MTA

docx L2a1. AGREEMENT about making Human Biological Material available to a Research Principal for an Action 10.0
pdf L2a1a. Example of wording regarding the transfer of conditions in L2a1 10.0
docx L2a2. AGREEMENT about making Human Biological Material available for an Action in clinical trials and performance studies 10.0
docx L2a3. AGREEMENT about making Human Biological Material available when a Research Principal sends samples for an Action to a Recipient 10.0
pdf K5. Information on agreements when human biological material is to be sent for an action 10.0

Research - Instructions

pdf K2.1 Form Selector 10.0
pdf K4. Instructions for completing form L1.1, L1.2 and L1.3 10.2
pdf K5. Information on agreements when human biological material is to be sent for an action 10.0
pdf L2a1a. Example of wording regarding the transfer of conditions in L2a1 10.0
pdf Ti5.1 Instructions for completing form T1.1 and T1.3 10.1
pdf Ti6. Selection of form for clinical trials 10.0

Staff - information

pdf B1. Glossary 10.1