US FDA unveils new pathway to approve personalized therapies

The U.S. Food and Drug Administration can approve new personalized treatments for rare and deadly genetic diseases based on ...
STAT

FDA chiefs offer roadmap to expand custom gene-editing treatments like Baby KJ’s

Marty Makary and Vinay Prasad offered a roadmap for expanding access to custom gene-editing treatments like the one used to ...

Handbag Designer Tyler Ellis Is Selling Her Stylish L.A. Home for $32 Million

Around nine years ago, Tyler Ellis doled out $12.3 million for a fairly plain French-inspired residence in the western ...
Washingtonian

How a Top DC Lawyer and High-Stakes Poker Player Risks Losing It All

Tom Goldstein lived a double life—and is now fighting federal charges for alleged financial crimes. Why did he risk it all to play cards?
JD Supra

Enforcing Trade Secrets across borders: A comparative look at the UK, EU, US, Australia and China - Co-ordinating enforcement across jurisdictions can present a complex web of ...

Trade secrets are increasingly recognised as vital assets in the intellectual property portfolios of modern businesses. Unlike patents or trade ...
JD Supra

FDA Signals Major Shift for QMSR Transition for Medical Device Applications

Drug & Device Team provides recommendations based on Food & Drug Administration (FDA) draft guidance on Quality Management System ...
Opinion
The LancetOpinion

Aligning SPIRIT and SAGER guidelines for equity in clinical trials

Recommendations for Interventional Trials (SPIRIT) 2025 guidelines published in The Lancet and commend the efforts to enhance transparency and rigour in clinical trial protocols.1,2 Accurate and ...