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ERNs

Open letter of the rare diseases community

An open letter signed by all ERNs calling for a renewed and continuous support to the ERNs was published.
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ERN-EYE, ERNs

First patients enrolled in REDgistry – July 2023

As of July 2023, the first patients have been enrolled in REDgistry, after giving their informed consent.
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ERNs

Introducing Together4RD’s newly published Position Statement on collaboration between ERNs and industry!

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ERNs, Events

Black Pearl Awards – It’s nominations time again!

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ERNs

ERICA Survey on ERNs and Clinical Research

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ERNs

Public Consultation on the Strategic Research & Innovation Agenda of the future European Rare Diseases Partnership

The Strategic Research and Innovation Agenda of the RD Partnership is now open for public consultation.
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ERNs, Events

EURORDIS Partnership Webinars: Rare Disease National Networks & ERN National Coordination Hubs

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ERN-EYE, ERNs

Development of the New CPMS – Business Implementation Group first meeting on 25th October

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ERN-EYE, ERNs, Publications

ERN-EYE Consensus Statement meeting for Bardet-Biedl Syndrome

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ERNs

Research Mobility Fellowships funding

The last round for the Research Mobility Fellowships funding opportunity will open on October, 3rd, 2022.
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