REF. E-MDR-MOD-01 – E-LEARNING
EUROPEAN REGULATIONS
REGULATION (EU) 2017/745
COURSE DESCRIPTION
The Overview of the European Medical Device Regulation module presents the vocabulary and general principles of Regulation (EU) 2017/745.
DURATION
23 minutes, including a 15-minute lesson and 8 minutes of quizzes
E-LEARNING
TECHNICAL PREREQUISITES
Computer and internet connection
METHODS USED
The module is composed of a lesson in the form of an interactive video with voice-off and learning activities. The module can be accessed 24/7. Reminders are sent to monitor knowledge acquisition and avoid a break in the learning curve.
TARGET TRAINEES
All individuals involved in the MD sector
PREREQUISITES
No prerequisite
ADDITIONAL BENEFITS
Summary presentation of the regulation
Support materials designed by experienced consultants-trainers
Interactive lesson
Short modules that can be accessed as often as required and autonomously
As an option, you may select Q&A sessions with one of our consultants-trainers
ACCESS
The CEISO ACADEMY platform can be accessed for a period of two months within two business days at most of approval of your order.
EDUCATIONAL GOALS
- Learn the vocabulary and scope of the Regulation
- Become familiar with the major points of the Regulation
- Become aware of the parties governed by the Regulation
COURSE CONTENT
Assistance with navigation/Module objectives/Presentation of the course content
- Definitions
- Scope
- Structure of the regulation
- Parties involved
EVALUATION METHODS
- Course evaluation quiz
- Satisfaction survey
- Attendance certificate
This training is assessed based on each individual’s acquisition of knowledge via a quiz at the end of the program (success criteria >= 80%). If trainees pass the quiz, they receive their training certificate, as well as the corrected quiz, by email.
