Topic: Data

Patient-reported Outcome Measures (PROMs) – what they are and why they matter

Cancer outcome research – what it is and why it matters

Collaborative multidisciplinary working within the hospital: the “oval table”

ESMO Checklist: General Quality Issues for Patient Treatment Workflow

Podcast on involving primary care in research

Podcast series on data and cancer registries

Guidance for Institutional Review Boards and Clinical Investigators

Real World Data in Oncology – Unicancer

The Cancer Trials Ireland Podcast

Overview of ISBER Best Practices Recommendations 2018

Common Minimum Technical Standards and Protocols for biobanks dedicated to cancer research – IARC Technical Publication No44

IARC Learning resources – biobanking

Article: “An introduction to starting a biobank”

Procedure – Creation of a specific research biobank

Procedure – Creation and organization of a general research biobank

Setting up a Cancer Centre: A WHO–IAEA Framework

Health Economics Analysis Plan for the SCIENCE study (Stem Cell therapy in IschEmic Non-treatable Cardiac diseasE)

Good practice in the use of Non Face-to-Face (remote) care channels

EORTC Policy on Data Sharing

Slovenian Cancer Registry – data usage information