Time to spotlight folks doing great work in R&D strategy and trial design, including excellence in AI, diversity, RWE, and patient-facing technology. Nominate them for the Citeline Awards; deadline is now March 1. https://t.co/J2VYLKBNQ5
A holiday gift for anyone wondering what I was up to for @PharmaScrip at #ASH24 a few weeks ago: one of my long reads about what’s happening in sickle cell disease is free to read without a subscription. https://t.co/uIGf4gbDxl
My comrade Brenda Sandburg several years ago profiled pioneering photojournalist Betty Steele, who died recently. Here’s an short – and wonderful – clip of Brenda interviewing Betty. Inspiring.
Join host @jrovner and panelists @shefalil, @SarahKarlin, and @AliceOllstein for a new health-packed ep. of #WTHealth! This week's discussion includes reproductive health, drug pricing, legislation for organ transplants, and more! https://t.co/kX5Lslmet0
My TrialScope colleagues are benchmarking how biopharmas balance clinical trial reporting compliance/transparency with redacting sensitive company & patient data. If you’re involved in this area, help us out by taking this brief confidential survey: https://t.co/Y1dRmzmXzI
Thomas Wicks, a Citeline colleague & trial transparency SME, is benchmarking how pharma is balancing transparency with needs to redact or anonymize some data. Help us out with our survey. #clinicaltrials#redaction#transparency
https://t.co/u8H5n9BVU3
Saudi FDA’s membership to PIC/s means that it can become a reference authority for inspecting pharmaceutical factories, reports @ScripFrancesca
https://t.co/oRm8Vuyb4x
Wow - only 6 voting members on panel, 2 of whom are regular members of the PCNSDAC. In all my many many years of covering adcomms have never seen a panel that small.
(1/2) An interesting look at the saga of Pepaxto from our @ScripFrancesca and @PinkSheetSutter today. This is Francesca's look at the EMA perspective ... #pinksheet#pharma: Oncopeptides’ Melflufen: Same Data, Different Conclusions From EMA, US FDA https://t.co/7pv87M3jJU
More supplemental filings from me and @SarahKarlin ... #pinksheet#pharma: Supplemental Filings: Pink Sheet Notebook On Disease Lobbying, Dan Leonard’s Next Act, And More https://t.co/4vGvoA0u6v
Our take on yesterday's big neurology news from @PinkSheetSutter ... #pinksheet#pharma: @US_FDA Neuroscience Office Director Billy Dunn Departs As Agency Faces New Review Challenges https://t.co/7ucRnd3ZZW
My analysis of the new OPT org chart ... #Pinksheet#Pharma: CBER’s New Home For Gene Therapies: OTAT Changes To OTP But Leadership Questions Remain https://t.co/wnzsf6qGS7
“We have these big societal issues and the decision about an individual product is like the tip of the spear of something that needs context,” @US_FDA's Robert Califf says about use of adcomms @SarahKarlin https://t.co/4pyOAlNgFD