This Rare Disease Day, PharmaTimes talks to @RaremarkHealth's Pete Chan about the myriad of stakeholders that make up the rare disease ecosystem: https://t.co/3uiVMuPuJI
#RareDiseaseDay - We’re posting stories on all our community pages today, highlighting how more than 300 million people are living with rare disease. “Rare is many. Rare is strong. Rare is proud.” @Rare Disease Day
Reaching those with a rare medical condition to move forward research requires a different approach @RaremarkHealth in @ContractPharma https://t.co/FOskWhuu6u
Rare Disease Day is a much-needed fixture in the calendar, but the job of delivering new treatments cannot be achieved in a big-bang, once-a-year burst of activity https://t.co/UT5vjMNQxr #RareDiseaseDay#rarediseaseday2020
Raremark announces new appointments.
Industry experts Neil Rotherham, Tim Davis and Jeremy Edwards have been appointed as Chairman, Chief Executive Officer and Chief Commercial Officer, to help the company accelerate progress in rare disease research.
https://t.co/GNl4ufLRYu
Raremark collaborated with Alex, The Leukodystrophy Charity (formerly ALD Life) to reveal the true impact of adrenomyeloneuropathy on people living with the condition. This is what we found.@alexTLCsupport
#leukodystrophy#raredisease
https://t.co/2S5S2xPxsY