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RARE News
RARE News
DREAMS: a new Horizon Europe project brings hope to rare disease patients
By admin
12 April 2024
Industry Insights
As we enter a new financial year, how does the UK Budget affect the rare disease community?
By CONTRIBUTOR
10 April 2024
RARE News
Multidisciplinary expert panel explores the necessity to “shed light” on rare and undiagnosed diseases: an invitation to attend a live event at Harvard Medical School, in-person or virtually
By admin
10 April 2024
RARE News
AKU Society launches Global Patient Registry to drive research into ultra-rare disease alkaptonuria
By admin
10 April 2024
RARE News
New report: If Only You Knew
By admin
10 April 2024
RARE News
Nxera Pharma joins the World Orphan Drug Alliance
By admin
9 April 2024
RARE News
Eurordis to host 12th European Conference on Rare Diseases and Orphan Products (ECRD 2024)
By admin
4 April 2024
RARE News
Miami community comes together for CureDuchenne, raising nearly $2.5M since 2021
By admin
3 April 2024
RARE News
SMA Europe launches its 12th call for research
By admin
3 April 2024
RARE News
Sickle Cell Disease Association of America promotes Kevin Amado Jr.
By admin
27 March 2024
Letters
How can we get the patient heard by the regulators?
By CONTRIBUTOR
27 March 2024
RARE REV-inar
Eight challenges in developing rare disease therapies
By editor
25 March 2024
RARE News
Rare Disease Day 2024 – Call for greater awareness of X-linked adrenoleukodystrophy and cerebral adrenoleukodystrophy
By admin
20 March 2024
RARE News
Rare disease advocates learn to accelerate therapeutic development at 9th RARE Drug Development Symposium
By admin
19 March 2024
RARE News
Alnylam launches Hereditary ATTR (hATTR) Amyloidosis campaign to help shorten diagnosis time
By admin
19 March 2024
RARE News
New primer highlights latest understanding of rare inherited disease alkaptonuria
By admin
19 March 2024
RARE News
DEBRA UK asks the British public to BE the difference for EB in 2024
By admin
19 March 2024
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