الوصف

Delegates participating in this course will:

  • Gain an overview of the critical changes with EU MDR and EU IVDR, and their implications
  • Find out about implementation timescales and their impact on resources
  • Discover what EU MDR and EU IVDR mean in practice


الأهداف

About the EU MDR and EU IVDR

 

The EU MDR and EU IVDR were published in the Official Journal of the European Union on May 5, 2017 as Regulation (EU) 2017/745 and Regulation EU (2017/746). The new rules will apply after a transition period of three years for MDR and five years for IVDR. These two eLearning courses will help medical device and In Vitro diagnostic device manufacturers understand the complex new regulations.


المستمعين

This course is intended for, but not limited to, regulatory personnel, managers, CEO, CFO, or any medical device or IVD field personnel who want to learn about the new regulations

مكونات حزمة

اختر عرضًا لكل مكون من مكونات الحزمة ، ثم انقر فوق الزر "إضافة إلى العربة" أدناه:

Introduction to the New EU Medical Device Regulation (MDR) eLearning Course

عروض

Introduction to the New EU Medical Device Regulation (MDR) eLearning Course

Introduction to the New EU In Vitro Diagnostic Regulation (IVDR) eLearning Course

عروض

Introduction to the New EU In Vitro Diagnostic Regulation (IVDR) eLearning Course

التفاصيل

44299412

EGP 6268.00 EGP 5118.00

حصة

يواجه النظام حاليًا مشكلات ونعمل على إيجاد حل لها. إذا واجهت خطأ ، فالرجاء العودة قريبًا وإعادة المحاولة.
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