# Commission Implementing Decision (EU) 2019/1396 of 10 September 2019 laying down the rules for the application of Regulation (EU) 2017/745 of the European Parliament and of the Council as regards the designation of expert panels in the field of medical devices (Text with EEA relevance), Division 3: For tasks referred to in Article 54(1) of Regulation (EU) 2017/745 and Article 48(6) of Regulation (EU) 2017/746, the maximum number of working days for which experts may be remunerated is set out in Table 1.

Extent: E+W+S+N.I.

Table 1
Maximum number of working days for which experts may be remunerated for tasks referred to in Article 54(1) of Regulation (EU) 2017/745 and Article 48(6) of Regulation (EU) 2017/746
advisors of the respective expert panel or sub-groups who validate the opinion or view produced by the rapporteur and the co-rapporteur
Regulation (EU) 2017/745Article 54(1)
Regulation (EU) 2017/746Article 48(6)
Decision on whether a scientific opinion should be developed (Yes/No)
Development and provision of a scientific opinion
Provision of a view of the performance of an in vitro diagnostic medical device
Chair/Vice-Chair
N/A
2
2
Rapporteur
1
5
4
Co-rapporteur
1
5
4
Reviewing members
N/A
0,5
0,5
Advisors assigned pursuant to Article 2(6) of this Decision
N/A
2
2

---
Source: https://www.legislation.gov.uk/eudn/2019/1396/annex/division/3 (the official version)
Page: https://openlegislation.uk/eu-decision-2019-1396/annex/division-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.