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How to set up a Multiple Sclerosis Registry? MSDA Academy Webinar Series
One of the key strategic objectives of the MSDA Academy is to promote trustworthy and transparent practices in the use…
EMSP joins new EU funded project called More-EUROPA
While randomized controlled trials (RCTs) remain the mainstay in drug development, approval, and reimbursement, the potential of real-world data (RWD)…
Tyrolean MS Society takes a new approach to exchanging information with „look and listen“
The COVID-19 pandemic heralded a time in which the Tyrolean MS society had to and was allowed to deal with…
MS Data Alliance Stakeholder Engagement Meeting 2022
On 16 November 2022 EMSP representatives (Herbert Temmes, Jana Hlaváčová, and Mohsharif Nasrulloeva) participated in the 2nd MS Data Alliance…
Presentation of the first Multiple Sclerosis Registry in Spain: EMDATA
About EMDATA The EMDATA (In English: MSDATA) project in Spain aims to collect and store information of interest on issues…
Italian MS Society launches collaboration with the National Civil Protection Service
The Italian MS Society (AISM) has recently signed a memorandum of understanding with the Department of Civil Protection in Italy, an…
