Are you a medical device company looking to navigate the European Union Medical Device Regulation (EU MDR) 2017/745 with ease? Look no further than our EU MDR Courses – the ultimate courses to help you understand and comply with this complex regulation.
With our EU MDR courses, you’ll learn everything you need to know about the EU MDR. From the basics of the regulation to more complex requirements, you’ll be an EU MDR expert in no time.
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Non-compliance with the EU MDR can result in hefty fines, legal action, and negative publicity. Our EU MDR Courses will help you understand the regulation and avoid these costly mistakes.
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About The Author:
Isabel Osorio is the president and founder of MDR Consultants Inc. , a medical device consulting firm specializing in regulatory and quality consulting services for the medical device industry. She is a former member of industry following a 16-year career in the medical device field, where she gained extensive experience as an Engineer, a Lead Auditor and a Certified Trainer for Notified Bodies, and as a medical device consultant. While working on the front lines as a Clinical Specialist years ago, a chance encounter opened her eyes to the detrimental effects of companies skipping past proper quality controls and procedures.
This experience changed her perspective on the importance of Medical Device Standards and Regulations forever and inspired her to focus her career on helping medical device companies and professionals better understand the requirements to ensure confidence and competence in their implementation of relevant requirements. Product malfunctions can have harmful effects on someone’s life, including death, and that patient could be you or a loved one. That is why patient safety is at the heart of her MDR Consultant’s mission to provide best-in-class training and consulting services. You can reach her at info@mdrconsultants.com