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Strategic Context of the Update The manual’s update is part of a continuous review process for the Manuals of Registration...
The medical device industry is undergoing an accelerated transformation. Technologies that seemed distant just a few years ago are now...
Measure Simplifies the Process for Good Manufacturing Practices Certification Regulatory Streamlining in Medical Device Manufacturing Certification The Brazilian National Health...
We are confirmed to participate in MEDICA 2025 with a clear objective: to connect international medical device manufacturers to the...
Unparalleled Global Scale and Relevance MEDICA isn’t just a trade show—it’s the world’s largest global marketplace for medical technology, uniting...
Introduction The Brazilian medical device market represents one of the most complex and dynamic regulatory environments in Latin America. With...
Introduction The Medical Device Single Audit Program (MDSAP) represents a paradigm shift in regulatory compliance for medical device manufacturers seeking...
Introduction The Brazilian medical device market presents significant opportunities for international manufacturers, but navigating the regulatory landscape requires expertise in...
Understanding the Medical Device Classification Framework The Foundation of Regulatory Compliance Medical device classification serves as the cornerstone of regulatory...
