The Food and Drug Administration (FDA) and Japan’s Pharmaceuticals and Medical Devices Agency (PMDA) met on Tuesday to optimize the facilitated review pathway (FRP) to expedite access to essential ...

GSK's revenue and EPS exceeded my expectations and those of analysts. Check out the reasons why I am upgrading GSK stock's ...

Discover Stoke Therapeutics' innovative RNA-based treatments like zorevunersen for Dravet syndrome, with a promising pipeline ...

The adoption of these standards is driven by regulators such as FDA and PMDA, who mandate that data must be submitted in these formats. This post gives a very brief overview of each model ...

About 250 have registered their products with internationally recognized agencies like Japan's Pharmaceuticals and Medical Devices Agency (PMDA) and the US Food and Drug Administration (FDA).

Focus on Patients with Elevated Markers of Heart Stress and Inflammation Procedural enhancement using FDA Approved Morph DNA ... associated with engaging Next PMDA Consultation after Review ...

AVITA Medical, Inc. (NASDAQ: RCEL, ASX: AVH), a leading therapeutic acute wound care company delivering transformative solutions, today reported financial ...

Hyderabad: Aurobindo Pharma has announced that the United States Food and Drug Administration (US FDA) had conducted an ...

Hyderabad: Aurobindo Pharma has announced that the United States Food and Drug Administration (US FDA) has concluded a ...

SID Medicos the South Korean cosmetics business developing advanced aesthetic solutions today announces a landmark moment in the company's growth, as it reaches global sales of 3 million vials. Total ...

To register for the presentation, please follow this Zoom link: https://us02web.zoom.us/webinar/register/WN_Nx3kCIIOSmOj686nctwpRA. A replay will be available on the AVITA Medical website, ...