Deliverables

Here you can explore the deliverables produced as part of the In Silico World project and those made publicly and freely available to the In Silico Medicine research community.


WP 1 – Coordination and Management

D1.1 – Risk analysis report
D1.2 – Risk analysis report

 

WP 2 – Development of advanced solutions

D2.1 – First report on Advanced solutions (Confidential)
D2.2 – Updated report on Advanced solutions
D2.3 – Final report on Advanced solutions

 

WP 3 – Validation Collections

D3.1 – Report on initial validation data collections (Download)
D3.2 – Report on the certification of validation data (Download)
D3.3 – Report on publication of validation collections

 

WP 4 – Technical Standards and Regulatory aspects

D4.1 – Guideline on model’s credibility standards
D4.2 – First report on the qualification activities (Confidential)
D4.3 – Updated report on the qualification activities
D4.4 – Final report on the qualification activities

 

WP 5 – Dissemination, Communication, and RRI

D5.1 – Dissemination and Communication Plan (Confidential)
D5.2 – Dissemination Report (Download)
D5.3 – Dissemination Report update
D5.4 – Dissemination Report update
D5.5 – Policy Brief
D5.6 – Information Package and Lecturing Materials
D5.7 – SWOT analysis process
D5.8 – White paper on Policies
D5.9 – ISW online Community of Practice and GSP consensus

 

WP 6 – Scalability and efficient computing

D6.1 – Requirements analysis report (Confidential)
D6.2 – Scalability strategies report
D6.3 – Efficiency recovery strategies report
D6.4 – Open Source software for rule-based data sharing

 

WP 7 – Re-training and Education

D7.1 – Report on ILOs, modules, and delivery modes (Confidential)
D7.2 – Report on training the IST workforce

 

WP 8 – Exploitation, ecosystem enlargement, and technology transfer

D8.1 – Exploitation plan
D8.2 – Report on Results’ Exploitation
D8.3 – Report on Results’ Exploitation (update)
D8.4 – Report on Persistence of ISW resources

 

WP 9 – Legal and ethical framework

D9.1 – Legal and ethical inventory (Download)
D9.2 – In-depth analysis of legal and ethical requirements
D9.3 – Implementation guidance and guidelines
D9.4 – Validation and recommendations for lawmakers and policymakers
D9.5 – Initial data management plan (Confidential)
D9.6 – Intermediate data management plan (Confidential)
D9.7 – Final data management plan

 

WP 10 – Ethics requirements

D10.1 – Research participants recruitment criteria
D10.2 – Informed consent procedures for human participation
D10.3 – Templates of informed consent/assent forms and information sheets
D10.4 – Copies of opinions/approvals by the ethics committee and/or competent authorities
D10.5 – Check if special derogations to the rights of data subjects have been established under local legislation (Confidential)
D10.6 – Host institution must confirm that it has appointed a Data Protection Officer (DPO) (Confidential)
D10.7 – Technical and organisational measures description to safeguard the rights and freedom of data subjects (Confidential)
D10.8 – Description of security measures to prevent unauthorised access to personal data or equipment (Confidential)
D10.9 – Description for anonymysation/pseudonymisation techniques (Confidential)
D10.10 – Explicit confirmation of lawful basis for further data processing (Confidential)