📢 Help spread the word by sharing this opportunity with your networks.
Find out more and apply 👉 rd-research.org.uk/uncategorize...
Deadline: 16 Nov
📢 Help spread the word by sharing this opportunity with your networks.
Find out more and apply 👉 rd-research.org.uk/uncategorize...
Deadline: 16 Nov
Find out more & apply 👉 rd-research.org.uk/uncategorize...
Application deadline: 16 Nov 2025
Find out more & apply 👉 rd-research.org.uk/uncategorize...
Application deadline: 16 Nov 2025
📣 Don’t miss out. Spread the word and share this with your networks!
🤝Do you know a young researcher who is or has meaningfully and effectively involved your community in their research?
Share this opportunity with your networks!
Find out more & apply tinyurl.com/ECRaward25
📣 Don’t miss out. Spread the word and share this with your networks!
🚀Find it in the rare disease section (p.160).
tinyurl.com/msue2nwc
🚀Find it in the rare disease section (p.160).
tinyurl.com/msue2nwc
📝 We’re looking forward to sharing the insights soon — watch this space for updates.
📝 We’re looking forward to sharing the insights soon — watch this space for updates.
📝UK-based researchers, PPIE members & rare disease advocates, read the recommendations & complete the survey here 👉 tinyurl.com/PPIEChange
📝UK-based researchers, PPIE members & rare disease advocates, read the recommendations & complete the survey here 👉 tinyurl.com/PPIEChange
🧬 If you know someone doing great work, encourage them to apply and help spread the word through your networks!
🤝Do you know a young researcher who is or has meaningfully and effectively involved your community in their research?
Share this opportunity with your networks!
Find out more & apply tinyurl.com/ECRaward25
🧬 If you know someone doing great work, encourage them to apply and help spread the word through your networks!
Register your interest: tinyurl.com/DystoniaIMPACT
Or contact the team at dystoniaimpact@qmul.ac.uk
Register your interest: tinyurl.com/DystoniaIMPACT
Or contact the team at dystoniaimpact@qmul.ac.uk
📝tinyurl.com/RDRLDproject
🔴 Deadline: 12 September
RDR UK & @lifearc.bsky.social are building a tool to map the rare disease research landscape — and your input matters!
Researchers, patients, families, carers & rare disease advocates — 📝please take the survey tinyurl.com/RDRLDproject
📝tinyurl.com/RDRLDproject
🔴 Deadline: 12 September
Deadline: 16 Nov 2025
🤝Do you know a young researcher who is or has meaningfully and effectively involved your community in their research?
Share this opportunity with your networks!
Find out more & apply tinyurl.com/ECRaward25
Deadline: 16 Nov 2025
RDR UK & @lifearc.bsky.social are building a tool to map the rare disease research landscape — and your input matters!
Researchers, patients, families, carers & rare disease advocates — 📝please take the survey tinyurl.com/RDRLDproject
RDR UK & @lifearc.bsky.social are building a tool to map the rare disease research landscape — and your input matters!
Researchers, patients, families, carers & rare disease advocates — 📝please take the survey tinyurl.com/RDRLDproject
🤝Do you know a young researcher who is or has meaningfully and effectively involved your community in their research?
Share this opportunity with your networks!
Find out more & apply tinyurl.com/ECRaward25
🤝Do you know a young researcher who is or has meaningfully and effectively involved your community in their research?
Share this opportunity with your networks!
Find out more & apply tinyurl.com/ECRaward25
🟢Deadline extended to 20 August as we are particularly keen to hear from across all four nations of the UK so we can build a truly representative understanding of the challenges and needs across different regions.
🖊️Take the survey tinyurl.com/r-dsurvey
🔎 Share your experiences with regulatory and market access pathways for rare disease — the good, the bad, and the changes that you would like to see!
📝Take the survey tinyurl.com/r-dsurvey
🟢Deadline extended to 20 August as we are particularly keen to hear from across all four nations of the UK so we can build a truly representative understanding of the challenges and needs across different regions.
🖊️Take the survey tinyurl.com/r-dsurvey
🖊️ If you haven’t had a chance to share your experience with UK regulatory pathways in rare disease research, there’s still time! Your insights can help drive change.
📝Take the survey tinyurl.com/r-dsurvey
🔎 Share your experiences with regulatory and market access pathways for rare disease — the good, the bad, and the changes that you would like to see!
📝Take the survey tinyurl.com/r-dsurvey
🖊️ If you haven’t had a chance to share your experience with UK regulatory pathways in rare disease research, there’s still time! Your insights can help drive change.
📝Take the survey tinyurl.com/r-dsurvey
👇Check out their article capturing the voices and priorities shared on the day.
👇Check out their article capturing the voices and priorities shared on the day.
Read it here: t.ly/Ka7qn
Read it here: t.ly/Ka7qn
👉Take a closer look at their work and poster tinyurl.com/UPNAT
👉Take a closer look at their work and poster tinyurl.com/UPNAT
🔎 Share your experiences with regulatory and market access pathways for rare disease — the good, the bad, and the changes that you would like to see!
📝Take the survey tinyurl.com/r-dsurvey
🔎 Share your experiences with regulatory and market access pathways for rare disease — the good, the bad, and the changes that you would like to see!
📝Take the survey tinyurl.com/r-dsurvey