by adminReaktio | Feb 20, 2025 | Medical Device Services
Understanding the Importance of BEP and BER in MDR Compliance Navigating the stringent requirements of the European Medical Device Regulation (MDR, EU 2017/745) requires a structured and comprehensive approach to biological evaluation. Two key documents essential to...
by adminReaktio | Feb 13, 2025 | Medical Device Services
Understanding the Biological Evaluation Report (BER) Ensuring the biological safety of a medical device is a crucial aspect of meeting the European Medical Device Regulation (MDR, EU 2017/745) requirements. At the heart of this process is the Biological Evaluation...
by adminReaktio | Feb 6, 2025 | Medical Device Services
Understanding the Biological Evaluation Plan (BEP) Ensuring the biological safety of a medical device is a fundamental requirement under the European Medical Device Regulation (MDR, EU 2017/745). A core component of this process is the Biological Evaluation Plan...
by adminReaktio | Jan 30, 2025 | FDA
Weighing Your Options: FDA vs. EU-MDR Choosing between FDA and EU-MDR approval is not just a regulatory decision—it’s a strategic choice that impacts your time-to-market, costs, and long-term compliance strategy. Each pathway presents unique benefits and challenges,...
by adminReaktio | Jan 23, 2025 | General
How FDA Approval Can Open Doors to International Markets Securing approval from the U.S. Food and Drug Administration (FDA) is a significant milestone for medical device manufacturers. Beyond allowing entry into the U.S. market, FDA approval can also serve as a...
