Course Outline

The objectives of the MDR.
Quality management system requirements in the MDR
Device classification and conformity assessment route in the MDR
Technical documentation requirements in the MDR
Clinical evaluation process requirements in the MDR
UDI and traceability requirements in the MDR
Postmarket surveillance.
Reporting requirements in the MDR
Life-cycle of products linked to risk management and clinical evidence.
Auditing impact of the MDR

Schedule & Fees

2026 Schedule & Fees

USD 2,600

Per participant

8 - 12 Nov, 2026
English

USD 2,600

Per participant

8 - 12 Nov, 2026
Arabic

2027 Schedule & Fees

USD 2,600

Per participant

24 - 28 Jan, 2027
English

USD 2,600

Per participant

24 - 28 Jan, 2027
Arabic

USD 2,600

Per participant

7 - 11 Feb, 2027
English

USD 2,600

Per participant

7 - 11 Feb, 2027
Arabic

USD 2,600

Per participant

25 - 29 Apr, 2027
English

USD 2,600

Per participant

25 - 29 Apr, 2027
Arabic

USD 2,600

Per participant

9 - 13 May, 2027
English

USD 2,600

Per participant

9 - 13 May, 2027
Arabic

USD 2,600

Per participant

25 - 29 Jul, 2027
English

USD 2,600

Per participant

25 - 29 Jul, 2027
Arabic

USD 2,600

Per participant

8 - 12 Aug, 2027
English

USD 2,600

Per participant

8 - 12 Aug, 2027
Arabic

USD 2,600

Per participant

24 - 28 Oct, 2027
English

USD 2,600

Per participant

24 - 28 Oct, 2027
Arabic

USD 2,600

Per participant

7 - 11 Nov, 2027
English

USD 2,600

Per participant

7 - 11 Nov, 2027
Arabic

‫Training Course in Implementing the EU’s Medical Device Regulation

Why Attend

Course Objectives

Course Outline

Schedule & Fees

2026 Schedule & Fees

2027 Schedule & Fees