Horizon 2020👥 Consortium Required (Min. 3 EU Countries)

Shortening the path to rare disease diagnosis by using newborn genetic screening and digital technologies → EURORDIS - RARE DISEASES EUROPE

Originally published in French
High language barrierEnglish translation available ↓

Opportunity overview

Recipient: EURORDIS - RARE DISEASES EUROPE • Role: participant • EC contribution: €736,895 • Project: SCREEN4CARE • Objective: In the EU alone, according to the Orphanet DB (https://pubmed.ncbi.nlm.nih.gov/31527858/), 30 million persons, 3,5-6% of the general population, are affe
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EU Fund Portal Signals

Is this worth the team's time?

Directional signals based on the call structure, available source text, and deadline pressure. These are not funding guarantees.

Source language: FrenchConfidence: Medium

Competition

4/ 5

Lower Competition

5 means a narrower, more approachable field. 1 means heavy competition.

Application Effort

1/ 5

Very Simple

1 is straightforward. 5 means a demanding application with heavier coordination or compliance.

Why competition looks like this

Confidence: Medium
  • The call looks specialized, which can narrow the field of credible applicants.

Why effort looks like this

Confidence: Low
  • Built from the available grant metadata and call structure.
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Consortium

Probably not required

Co-funding

Not clearly indicated

Documentation

Low

Deadline pressure

Closed

Eligibility scope

Narrow

Technical depth

Low

Plain-English translation

The original call appears to be in French. Translate the source summary and eligibility notes into concise English for faster review.

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Eligibility

Awarded

Application deadline

13/10/2021
Deadline expired

Key information

Value of call
€737k
Sector
Other
Country
FR
Funder
European Commission (Horizon 2020)

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Tracked by EU Fund Portal since 21/09/2026
Last checked 21/09/2026

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