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Course description
The course goal is to provide you with the right skills to follow the right path in getting the CE mark for your products. It covers all the areas of knowledge that a person needs such as having a greater insight into the overall regulatory process of registering medical devices in Europe and obtaining a CE mark and many more. The course uses different ways of delivering knowledge like case studies, videos, exercises, and individual tests. At the completion of the course, the skills that YOU will have are practical, applicable, and implementable. You can find the course outline in the video above
What you'll learn
- Participants will have greater insight into the overall regulatory process of registering medical device in Europe and obtaining a CE mark
- Participants will become better knowledgeable in medical device classification and understanding the quality management ISO 13485 related to CE mark certification
- Participants will become familiar with the different requirements for technical file preparation of medical device as part of its CE Mark certification in the European market
- Participants will be acquainted with the different key players involved the CE mark process and will comprehend the final steps needed to complete the CE mark certification
Instructor: Dr. Samer Sowidan
- Duration: 14 Hrs. Two Days
- Time: 9.00 am-4.00 pm
- Prerequisite for this course: None
- Language: English
- Level: Management or any one interested
- Classroom or Vitual Training
- Price US $ 495
- Certificate of completion is provided
- Discount available for companies who send three or more participants
- Seats for this course: 12
- Virtual through zoom or google meet
- Classroom course at Upbeat office, hotel or at the customer premises
