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CASRAI
Data Governance & Open Science

DMP Guide: MSCA for Biomedical Science

Learn how to design a fully compliant Data Management Plan (DMP) that satisfies Marie Skłodowska-Curie Actions open-data policies. Explore optimal file formats, metadata mapping, and repository selection for Biomedical Science research data.

1. Funder Policy & Open Data Compliance

In alignment with international open-science mandates, Marie Skłodowska-Curie Actions requires all principal investigators to submit a comprehensive Data Management Plan (DMP) with their grant application. A robust DMP details how research data will be collected, processed, documented, stored, shared, and preserved both during and after the project.

Funder-Specific Mandate Directive

The **Marie Skłodowska-Curie Actions (MSCA)** requires a comprehensive DMP as a formal deliverable for **Biomedical Science** studies due within Month 6 of project kickoff. Data must be made open under the standard principle: "as open as possible, as closed as necessary" to protect intellectual property.

Verified Funder Open-Science Portfolio

Based on independent, open-science bibliometric data from OpenAlex, the Marie Skłodowska-Curie Actions (MSCA) oversees a massive scholarly ecosystem with over 43,842 published research outputs under their funding catalog, accumulating over 1,202,144 citations across the global scientific record. To protect the public's investment in this massive knowledge corpus, the funder strictly enforces FAIR data management and open repository deposits, making compliance with this DMP protocol mandatory for all awarded grants.

For projects in the field of Biomedical Science, managing data correctly is essential not only for compliance, but also to support peer-review validation and reproducibility. All DMPs must be submitted through the Funding & Tenders Portal portal, using standard institutional guidelines.

2. Data Types, Formats, and Metadata Standards

A high-quality DMP must explicitly identify the types of data that will be generated and specify open, non-proprietary file formats to ensure long-term usability. For Biomedical Science, datasets typically range from raw observational measurements to curated computational models.

Biological data streams for **Biomedical Science** focus on cellular imaging and experimental protocols. The DMP specifies long-term archival plans, structured indexing mapped to the **Diseases Category** terminology, and secure patient anonymisation to satisfy **MSCA** auditors.

To guarantee discoverability, datasets should be documented using standardised metadata schemas that map to the Diseases Category branch of scholarly vocabularies. This ensures indexers and crawlers can crawl and identify research outputs accurately.

DMP ComponentCustom Target Value for Biomedical Science
Preferred File FormatsDICOM (microscopy files), HDF5 (cellular screens), XML (assays), CSV (tabular logs)
Metadata Schema StandardBioschemas, ISA-Tab (assay metadata), Dublin Core Metadata Standard
Target Scientific RepositoriesBioImage Archive, Zenodo, Dryad, and directory servers mapped in PubMed & MEDLINE

3. Step-by-Step DMP Construction Protocol

When preparing your DMP for a MSCA proposal, structure your document around these core sections:

  1. Data Collection and Generation:
    Describe the methodology, instrumentation, or software used to collect or generate new data. Detail quality assurance and quality control measures implemented at your facility.
  2. Documentation and Metadata:
    Explain how the data will be documented, including accompanying read-me files, data dictionaries, and laboratory notebooks. Specify the metadata standards to be utilized (using Bioschemas, ISA-Tab (assay metadata), Dublin Core Metadata Standard as standard).
  3. Ethics, Intellectual Property, and Consent:
    Address how sensitive or confidential datasets will be handled. Detail anonymisation processes, access controls, and compliance with institutional ethics boards.
  4. Storage, Backups, and Security:
    State where data will be stored during active research. Detail automated backup schedules, server redundancies, and access authorisation protocols.
  5. Long-Term Preservation and Archiving:
    Select the digital repository for post-project archiving (such as BioImage Archive, Zenodo, Dryad, and directory servers mapped in PubMed & MEDLINE). Confirm that the repository supports persistent identifiers (handles/DOIs) and provides secure preservation.

Open Science Workflows, Data Curation & Repositories

When drafting a data management plan dmp to satisfy MSCA guidelines, defining systematic data collection methods and formal data curation standards is vital. Utilizing institutional dmptool workflows ensures that these administrative requirements are built-in from the outset of the study. This includes describing protocols for data cleaning, validating data integrity via checksums, and conducting secure data wrangling on raw source files. Each output dataset must be documented with an explanatory data dictionary mapping key metadata fields. Architecturally, teams can configure either a secure relational data warehouse or a cost-effective cloud-based data lake, evaluating how this data lake vs data warehouse setup supports formal data analysis and immediate exploratory data analysis under MSCA guidelines. PIs will facilitate public sharing by leveraging the dryad data repository, creating searchable figshare datasets, or completing a zenodo data upload, ensuring tracking through the data citation index in compliance with nsf data management plan protocols and Marie Skłodowska-Curie Actions targets. The study will document clear data versioning protocols hosted on the open science framework osf to enable reproducible data sharing matching top fair data principles examples. Furthermore, any community-engaged data must respect the care data principles and support indigenous data sovereignty care standards to ensure local governance of shared knowledge under MSCA audits. Implementing this storage layout satisfies compliance protocols overseen by the MSCA data audit team.

4. Frequently Asked Questions

Are we required to share all raw data from our research?

No, MSCA policies generally recognise that some data cannot be shared publicly due to privacy, security, intellectual property, or commercialisation constraints. In such cases, your DMP must justify why certain datasets are restricted and describe how metadata will still be made discoverable.

Who owns the research data generated under this grant?

Data ownership is typically held by the host institution, subject to co-ownership clauses in collaborative projects. However, MSCA guidelines require that data be made as openly available as possible under open licensing, such as Creative Commons or Open Data Commons.

DMP Specifications

Funding BodyMSCA (European Union)
Submission ToolFunding & Tenders Portal
Crossref Funder ID100010665
Discipline FocusBiomedical Science
Target Index DBPubMed & MEDLINE

FAIR Principles

Your plan must align with the FAIR Principles:

  • Findable: Rich metadata and persistent DOIs.
  • Accessible: Free retrieval via standard protocols.
  • Interoperable: Open formats and vocabulary alignment (such as Bioschemas, ISA-Tab (assay metadata), Dublin Core Metadata Standard).
  • Reusable: Clear data licensing and reuse guidelines.

Referenced across the research world

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