Peter Marks, CBER director (Jim Lo Scalzo/Pool via AP Images)
October 16, 2024 01:35 PM EDT
FDA+

FDA lead­ers kick off rare dis­ease hub to in­crease cross-cen­ter col­lab­o­ra­tion

Zachary Brennan

Senior Editor

FDA of­fi­cials, in­clud­ing the di­rec­tors of CBER and CDER, on Wednes­day launched a rare dis­ease in­no­va­tion hub at a

Endpoints News

Sign up to read this article for free.

Get free access to a limited number of articles, plus choose newsletters to get straight to your inbox.

BECOME A PREMIUM SUBSCRIBER
ENDPOINTS CAREERS

Director of IT, Security

Viridian Therapeutics

Waltham, MA, USA

TRENDING NOW

Fac­ing a crit­i­cal week, Pfiz­er con­fronts an un­spar­ing foe in Star­board

FDA places hold on No­vavax's Covid-flu and stand­alone in­fluen­za vac­cines

First clin­i­cal test of RNA edit­ing re­stores miss­ing pro­tein in ge­net­ic dis­ease, Wave says

Q&A: Sanofi’s R&D head re­flects on his first year, a post-Dupix­ent fu­ture, and find­ing an iden­ti­ty

Take­da parts ways with Wave Life Sci­ences even with Hunt­ing­ton’s tri­al win

sponsored

Join the Gen­Script Biotech Glob­al Fo­rum: Un­lock­ing In­no­va­tions in Cell and Gene Ther­a­pies

A service from the Financial Times