Medical Device Adverse Event Reporting Regulations: EU vs. US FDA
Regulatory authorities in both Europe and the United States requir...
Effective Clinical Overviews: Regulatory Submissions
The Clinical Overview is a pivotal component of the Common Technic...
Rise in Digital Therapeutics and At-Home DiagnosticsÂ
Digital Therapeutics (DTx) is a subdivision of digital health, whi...
Clinical Research Organisations in Advancing Drug & Device Development
Clinical Research Organisations (CROs) are essential contributors ...
Pharma/Biotech – USA, Europe and Asia Regulatory Updates Roundup – Jan 2025
USA
FDA Approves Novel Non-Opioid Treatment for Moderate to Severe...
The Evolution of Medical Writing: Trends and Innovations in the Industry
Medical writing has long been an essential pillar of the healthcar...
