BluePrintOrphan's profile picture. Proven excellence in #orphandrug data analytics, forecasting, ​and market access strategy with a special focus in #RareDiseases *retweets/likes ≠ endorsements*

BluePrint Orphan

@BluePrintOrphan

Proven excellence in #orphandrug data analytics, forecasting, ​and market access strategy with a special focus in #RareDiseases *retweets/likes ≠ endorsements*

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Have you been wondering how #COVID19 will affect #orphandrug development? Check out our latest blog post about the pandemic’s impact on the #raredisease sector blueprintorphan.com/development/co…

BluePrintOrphan's tweet image. Have you been wondering how #COVID19 will affect #orphandrug development? Check out our latest blog post about the pandemic’s impact on the #raredisease sector blueprintorphan.com/development/co…

Highlighting our Patient Subtyping capabilities this month. Want to know more? Contact our team today! #raredisease #orphandrug

BluePrintOrphan's tweet image. Highlighting our Patient Subtyping capabilities this month. Want to know more?  Contact our team today! #raredisease #orphandrug

Curious about #raredisease treatment development progress in 2020? Check out some of this year's drug approvals! pharmaceutical-technology.com/features/treat…


Great to see everyone on screen at day 1 of Inborn Errors of Metabolism today! Looking forward to more discussion tomorrow #RareDiseases inborn-errors.com


Interesting read on how machine learning can be used to help fight #rarediseases pharmalive.com/machine-learni…


BluePrint Orphan reposted

The #NORDSummit will bring #raredisease leaders & stakeholders together to provide new approaches & fresh perspectives on #publicpolicy, clinical trials, access to #diagnostic testing & pharmaceutical innovation. Register or apply for a scholarship: bit.ly/2WJ7ziE

RareDiseases's tweet image. The #NORDSummit will bring #raredisease leaders & stakeholders together to provide new approaches & fresh perspectives on #publicpolicy, clinical trials, access to #diagnostic testing & pharmaceutical innovation. Register or apply for a scholarship: bit.ly/2WJ7ziE

BluePrint Orphan reposted

Join our experts for a free webinar: The Value of Orphan Drug Designation in your Drug Development Program ow.ly/9KBx50AmOra #OrphanDrug #RareDisease #ClinicalDevelopment #Regulatory #FreeWebinar #ClinialTrials #ClinicalStudies #Innovation Cato Research

Allucent_CRO's tweet image. Join our experts for a free webinar: The Value of Orphan Drug Designation in your Drug Development Program
ow.ly/9KBx50AmOra
#OrphanDrug #RareDisease #ClinicalDevelopment #Regulatory #FreeWebinar #ClinialTrials #ClinicalStudies #Innovation Cato Research

BluePrint Orphan reposted

With the #DISORDER: The #RareDisease Film Festival postponed by the pandemic, the Rare Outreach Coalition decided to start its own streaming channel and bring their content right into your home! Read more: bwnews.pr/2Obbpww


BluePrint Orphan reposted

LAST CALL to register for #RareAcrossAmerica Check out this article from @healourskin where Shannon von Felden, #RDLA program director, shares everything you need to know about this unique event. issuu.com/healours…/docs/ippf-100-spring-20-issuu/26


Interesting article on the discovery of novel genetic causes of #rarediseases healtheuropa.eu/genome-sequenc…


BluePrint Orphan reposted

Join #NORD, @CPathInstitute, @US_FDA and @TakedaPharma tomorrow, June 24 at 2:00 PM ET for “Shortening the Timeline for Developing New Treatments – How the Rare Disease Cures Accelerator–Data and Analytics Platform Can Help.” Register: bit.ly/2Bxd10k #RDCADAP #webinar

RareDiseases's tweet image. Join #NORD, @CPathInstitute, @US_FDA and @TakedaPharma tomorrow, June 24 at 2:00 PM ET for “Shortening the Timeline for Developing New Treatments – How the Rare Disease Cures Accelerator–Data and Analytics Platform Can Help.” Register: bit.ly/2Bxd10k #RDCADAP #webinar

Excited to see new funding opportunities for #raredisease research 🎉

The National Organization for Rare Disorders (NORD) is pleased to announce new funding opportunities through the Jayne Holtzer #RareDisease #Research Grants Program. Submission of proposals are due by August 25. Read more: bit.ly/2ANmLDO



Congrats to #ProtagonistTherapeutics on receiving #OrphanDrug Designation for hepcidin mimetic PTG-300

The National Organization for Rare Disorders (NORD) is pleased to announce new funding opportunities through the Jayne Holtzer #RareDisease #Research Grants Program. Submission of proposals are due by August 25. Read more: bit.ly/2ANmLDO



Today until July 31, the @US_FDA is seeking comments and feedback from patients, health professionals, and others in the #raredisease community to establish a clinical trials network federalregister.gov/documents/2020…


Interesting read on how #orphandrug biotech @Pharnext plans to respond to #COVID19 by leveraging AI data forbes.com/sites/lawrence…


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