Content Type: Guidelines

Establishment and operation of a tumour board

Preclinical Studies and Clinical Implementation in Phase I Studies

Intellectual Property (IP) and commercialisation

Working with your Tech Transfer Office

Policy on grant applications (EORTC)

Writing a grant – webinar

How to write a grant – webinar

European Code of Conduct for Research Integrity

Informed consent – SOP recommendations

Data Transfer Agreement – guidelines for development

Data Transfer Agreement – template

How to run phase 1 studies – podcast

Framework for evaluating and prioritizing medical equipment requests -case study

Collaboration model for Medical Technical Equipment system solutions – case study

Standard Operating Procedure: Internal Audits

Patient safety – e-learning

Developing guideline-based quality indicators (QIs)

Planning and delivering training programmes – template

The Importance of Your Participation in Health Care A Call to Action for Healthcare Professionals

Interface Working Group (IWG) foundational document – template