Why regulatory and quality due-diligence is often overlooked.
Shift the odds in your favor.
Take a metadata-driven approach to information management.
Product architects are challenged to address security throughout the device lifecycle.
Having trained biomedical equipment technicians in developing regions can help, but lack of funding is perpetuating a dire situation.
Inspections are inevitable. If you receive 483s, follow these tips to quickly and adequately respond to the agency.
What can we learn about how new technologies become eligible for additional payment?
Risk Management is the single most important topic impacting the medical device industry today.
Lasers have become a universal tool in medicine.
Change is constant, and we continue to evolve.