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Training4CRM project deliverables

The page lists 10 deliverables related to the research project "Training4CRM".

 List of Deliverables

Training4CRM: list of downloadable deliverables.
title and desprition type last update

Individual ESR public engagement plans / impact report

Dissemination to policy makers, end-users and the general public is the focus of the two public engagement workshops (research schools M12 and M18) where ESRs will make individual plans for appropriate activities. Activities should be relevant to the work of the ESR and be customised to the targeted audience. Activities may include taking part in DTU Science Programme for high school students, creating a 1 week, summer school for high school students, participation in Researchers’ Night, writing popular scientific articles in different magazines/newspapers, blogs, social media groups, IFLScience/Science Channel, YouTube etc. ESRs may be Marie Sklodowska-Curie Ambassadors. The Public Engagement Plans must be approved by the SB and the CEC. The plan must be revised M48.

Programme: H2020-EU.1.3.1. - Topic(s): MSCA-ITN-2016

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Documents, reports 2020-01-24

Project logo and templates

The Coordinator will create a project logo and relevant templates (ppt, poster, mail banner). All beneficiary and partner logos, the EU emblem and all templates will be readily available at the Training4CRM intranet.

Programme: H2020-EU.1.3.1. - Topic(s): MSCA-ITN-2016

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Documents, reports 2020-01-24

Necessary approvals and permits obtained and submitted to the Commission

For HUMAN EMBRYOS/FOETUSES (after GA) :
1. All the Human Pluripotent Stem Cells lines to be used must be registered in hPSCreg, copy of registration must be provided to REA
2. Human Neural Stem Cell lines lines to be used must be registered in hPSCreg ; copy of registration must be provided to REA
3. The project must be registered in hPSCreg and copy of this registration must be provided to REA

For HUMAN CELLS / TISSUE (after GA, before the commencement of the research work) :
1. Copies of ethical/regulatory approvals must be submitted prior to the start of the relevant research activities.

For ANIMALS (after GA, before the commencement of the research work):
1. Copies of ethical / regulatory approvals for the work to be carried out with animals must be submitted prior to the start of the relevant research activities.
2. Copies of personal licences and training certificates for the work to be carried out with animals (as indicated in the Part B Ethics Section) must be submitted prior to the start of the relevant research activities. If licences or training certificates expire during the course of the research, renewed documentation must be submitted in due time.

For THIRD COUNTRIES (throughout the project):
1. The applicant must confirm that the ethical standards and guidelines of Horizon2020 will be rigorously applied, regardless of the country in which the research is carried out
2. The ethics advisor shall report about the H2020 compliance of third country partners to the project.

For ENVIRONMENT PROTECTION AND SAFETY (after GA, before the commencement of the research work):
1. If relevant, copies of facilities authorisations must be provided (security classification of laboratory).
2. The applicant must ensure that appropriate health and safety procedures conforming to relevant local/national guidelines/legislation are followed for staff involved in this project.

For OTHER ETHICS ISSUES (throughout the project):
1. The Ethics coordinator must report to the REA with the periodic reports and the final report, and whenever it is considered to be necessary by the Ethics coordinator.
2. A complete portfolio of copies of all ethical approvals that cover all aspects of the research by all of the partners of the Consortium throughout the lifetime of the project must be compiled and retained by the Ethics Advisory and must be available to the REA if requested and for Ethics Checks or Audits.

Programme: H2020-EU.1.3.1. - Topic(s): MSCA-ITN-2016

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Documents, reports 2020-01-24

Final program for research school on Pre-clinical studies

Final program for research school on Pre-clinical studies incl. venue, lecturers, speakers etc

Programme: H2020-EU.1.3.1. - Topic(s): MSCA-ITN-2016

download deliverable 

Documents, reports 2020-01-24

Final program for research school on Micro- and Nanoengineering

Programme for research school on Micro- and Nanoengineering, incl. venue, speakers, lecturers etc.

Programme: H2020-EU.1.3.1. - Topic(s): MSCA-ITN-2016

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Documents, reports 2020-01-24

Final program for research school on Biotechnology

Competed program for research school on Biotechnology, incl. venue, speakers, letcurers etc

Programme: H2020-EU.1.3.1. - Topic(s): MSCA-ITN-2016

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Documents, reports 2020-01-24

Publish Training4CRM website

The Coordinator and the Communication and Exploitation Coordinator (UB) will create an appropriate structure for the Training4CRM website. The structure must take into account the different stakeholders. Every 3 months we will make a website visitor report to monitor number and behaviour of visits on Training4CRM website. These statistics will give us important pointers to continuously improve the website to fulfil its purpose of disseminating Training4CRM results to different audiences. DTU will host and maintain the website.

Programme: H2020-EU.1.3.1. - Topic(s): MSCA-ITN-2016

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Websites, patent fillings, videos etc. 2020-01-24

Establish Supervisory Board

The Supervisory Board (SB) includes one key representative from each beneficiary. Members of the SB must function as supervisor forat least one ESR. The SB is part of the management of the project,and also has tasks related to WP5 on training and education.

Programme: H2020-EU.1.3.1. - Topic(s): MSCA-ITN-2016

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Documents, reports 2020-01-24

Supervision team approval report

As the ESR are recruited the recruiting organisation must immediately create a supervision team (SUP) of 3 people, incl. a main supervisor from an academic beneficiary (from recruiting host or secondment host) and 2 co-supervisors, whereof at least one must be from an industrial beneficiary or partner. All SUPs must be approved by the SB and the Training Coordinator. For ESRs recruited M12 the report will be updated M13.

Programme: H2020-EU.1.3.1. - Topic(s): MSCA-ITN-2016

download deliverable 

Documents, reports 2020-01-24

Establish plan for network-wide meetings

The SB will at the kick-off meeting decide on a plan for network-wide meetings throughout the project

Programme: H2020-EU.1.3.1. - Topic(s): MSCA-ITN-2016

download deliverable 

Documents, reports 2020-01-24