Developing a drug delivery device requires strategic early-stage investments to ensure long-term success and cost efficiency. This whitepaper highlights six critical areas essential for the successful ...
Examining the evolving dynamics between EU and FDA regulations for medical devices. The webinar will address the historical practice of obtaining a CE Mark in Europe first, contrasting it with the ...
The intersection of healthcare and cybersecurity has become a critical bridge in safeguarding patient data and ensuring the integrity of medical technologies. Unpack the complexities of Section 524B, ...