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Ethics oversight

3

Ethics advisors and ethics advisory boards. Roles and function in EU-funded projects
Ethics appraisal process for EU-funded projects
EU-Funded projects: Ethics requirements and ethical oversight

Infectious diseases

1

COVID-19 research

Data governance

4

Code of practice for scientific research under the GDPR
Data protection
Data Protection Impact Assessments (DPIA): Tools and resources
International data sharing: Material Transfer Agreements and Data Transfer Agreements

Artificial intelligence and digital innovation

2

Artificial intelligence in biobanking and biomedical research
Ethics of AI Lab

Incidental findings

1

Incidental findings

Oncology

3

Cancer survivorship
Digital ELSI services for cancer research
Enhancing patient engagement in oncology research

Genomics

4

Access and benefit sharing of genetic resources
Organoids
Polygenic Risk Scores (PRS)
The rights of family members of genomic data

Sex and gender

1

Sex and gender in biomedical research

Participant rights, inclusion and engagement

4

Biobanking with children
Public and Patient Involvement and Engagement (PPIE) in biobanking
Reimbursement and compensation to research participants
Vulnerability in biomedical research: A broad spectrum

Biobanking and translational research practices

5

Biobanking research
Biobanks and One Health approach
Different types of biobanks
Digitalisation of biobanks
Governance structures for biobanks

Practical guidance on research data governance

3

How to conduct a Data Protection Impact Assessment (DPIA): A step-by-step approach
How to manage personal data in a new project
Preparation of a new project – what to do with the data

Practical guidance on data requests and access procedures

1

How to respond to personal data requests

Practical guidance on paediatric participation and engagement

1

A step-by-step engagement process for children in biobanking

Practical guidance on biobanks

2

Best practices for biobanking
How to set up a biobank

Quality standards

30

BBMRI-ERIC liaisons with international standardisation organisations
BBMRI.ch Swiss Biobanking Platform quality manual
BBMRI.de QM biobank manual
BBMRI.pl QM biobank manual
Biobanks Europe: Special issue on quality
Biotechnology – Biobanking – General requirements for biobanking (ISO 20387:2018)
CEN standards: Molecular in vitro diagnostic examinations and specifications for pre-examination processes for human specimen
CEN standards: Molecular in vitro diagnostic examinations and specifications for pre-examinations processes for circulating tumor cells (CTCs) in venous whole blood
CEN standards: Molecular in vitro diagnostic examinations and specifications for pre-examinations processes for exosomes and other extracellular vesicles in venous whole blood
CEN standards: Molecular in vitro diagnostic examinations and specifications for pre-examinations processes for urine and other body fluids
CEN standards: Molecular in vitro diagnostic examinations and specifications for pre-examinations processes for venous whole blood
Interoperability tools
ISO standards: Auditing
ISO standards: Biotechnology
ISO standards: Data quality / Data security
ISO standards: Laboratories for testing and calibration and medical laboratories
ISO Standards: Molecular in vitro diagnostic examinations and specifications for pre-examination processes for frozen tissue
ISO standards: Molecular in vitro diagnostic examinations and specifications for pre-examinations processes for formalin-fixed and paraffin-embedded (FFPE) tissue
ISO standards: Molecular in vitro diagnostic examinations and specifications for pre-examinations processes for saliva
ISO standards: Molecular in vitro diagnostic examinations and specifications for pre-examinations processes for venous whole blood
ISO standards: Molecular in vitro diagnostic examinations and specifications for pre-examinations processes in metabolomics
OECD best practice guidelines for biological resource centres
Preanalytical conditions to prepare human DNA from FFPE Tissue for Next Generation Sequencing (NGS)
Preanalytical conditions to prepare human DNA from whole blood
Preanalytical conditions to prepare human RNA from whole blood
Quality management systems – Requirements (ISO 9001:2015)
Sampling, storage and handling standards, consent procedures and templates
Summary and review of collected SOPs from project partner and literature
User satisfaction survey template
WHO/IARC Common minimum technical standards and protocols for biological resource centres dedicated to cancer research

Consent

1

Consent in biobanking

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