Welcome to Egmeditech
Join our 2nd Medical Device Conference June 2025
What We 'll Cover
Key Topics of Discussion
MDR and IVDR Updates:
Stay informed on the latest updates and regulatory changes surrounding the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR), ensuring compliance with evolving standards and enhancing the safety and effectiveness of medical devices and diagnostics.
Clinical Evaluation: How to Perform It:
Understand the essential steps in conducting clinical evaluations, including the systematic assessment of medical devices to ensure their safety, performance, and compliance with regulatory requirements, while aligning with global standards.
Usability
Explore the importance of usability in medical devices, focusing on designing products that are intuitive and user-friendly to ensure optimal performance, reduce errors, and enhance patient safety across diverse healthcare settings.
Biocompatibility:
Learn about the significance of biocompatibility in medical devices, focusing on the evaluation and testing of materials to ensure they do not cause adverse reactions when in contact with the human body, promoting patient safety and device longevity.
Risk Assessment:
Gain insights into the process of risk assessment in the development of medical devices, identifying potential hazards and implementing strategies to mitigate risks, ensuring that products meet the highest standards of safety and reliability.
Networking Opportunities with Industry Leaders and Regulators:
Engage in valuable networking opportunities with key stakeholders, including industry leaders and regulatory experts, to exchange knowledge, foster collaboration, and stay ahead of emerging trends and regulatory changes in the medical device sector.
Moments From First Edition
After the success of the first edition of the Medical Devices Conference, stay tuned for the second conference with medical device pioneers.
