PAPA-ARTIS project deliverables
The page lists 7 deliverables related to the research project "PAPA-ARTIS".
List of Deliverables
| title and desprition | type | last update |
|---|---|---|
Ethical guidance documentA discussion of ethical questions ranging from the risk/benefit considerations of the coiling and waiting period after staging to dealing with incidental findings in CT/MRI scans will be presented in this report. The standpoint of the Trial Steering Committee, the ethics boards and the competent authorities will be presented. Programme: H2020-EU.3.1.3. - Topic(s): SC1-PM-09-2016 |
Documents, reports | 2020-01-23 |
Links with existing projects/professional bodiesA list of existing, planned and potential links with existing projects/professional bodies will be provided. Programme: H2020-EU.3.1.3. - Topic(s): SC1-PM-09-2016 |
Documents, reports | 2020-01-23 |
PAPA-ARTiS Project Management HandbookPAPA-ARTiS Project Management Handbook †including programme of meetings, communication processes and roles and responsibilities of partners Programme: H2020-EU.3.1.3. - Topic(s): SC1-PM-09-2016 |
Documents, reports | 2020-01-23 |
Communication strategyA plan will be delivered as to how communication with the public, e.g. with a web-site, press releases and newsletters will be put into effect. Policy makers and regulators are also a target audience and particular strategies for communication with them will also be described. Programme: H2020-EU.3.1.3. - Topic(s): SC1-PM-09-2016 |
Documents, reports | 2020-01-23 |
Project Data Management PlanA project management handbook will be prepared which sets out the internal communication plan, meeting schedules and expectations of partners to support the described project management processes. Programme: H2020-EU.3.1.3. - Topic(s): SC1-PM-09-2016 |
Documents, reports | 2020-01-23 |
Trial registrationTrial registration Programme: H2020-EU.3.1.3. - Topic(s): SC1-PM-09-2016 |
Other | 2020-01-23 |
Clinical Trial Data Management planThe Clinical Data Management Plan is a document that describes which clinical data will be acquired and how it will be handled, stored, checked for consistency and plausibility, cleaned, and made available for the final analysis. The document will also describe how the data will be preserved after end of the project, and possibly made available for further research. Programme: H2020-EU.3.1.3. - Topic(s): SC1-PM-09-2016 |
Documents, reports | 2020-01-23 |