Das Online-Seminar findet in 8 Monaten, am 12.03.2024 von 09:00 – 12:00 Uhr statt.

PRRC “person responsible for regulatory compliance” I

Zielgruppe und Vorkenntnisse

The seminar is aimed at employees of medical device manufacturers from risk class I. We do not recommend any specific prior knowledge, but the following prior knowledge is advantageous:

  • Role and Activity at a medical device manufacturer or EC-REP
  • Experience as a QM- or RA-representative or Tech Doc Manager
  • (Internal) auditor or consultant for medical device manufacturers or EC-REP

Inhalte

Regulatory Requirements for the responsible person
Contents of the technical documentation
The conformity assessment procedure
Tasks and integration in the QM system

Ermäßigungen

Customer discount: mdc customers receive a 10% discount on the net price.

 

Hinweise

Please note that the registration fee and the associated participation only applies to one person. If several people take part in the seminar (remotely) even though only one person has registered, we reserve the right to exclude them from the seminar.

Preis pro Teilnehmer

450.00 Euro (zzgl. ges. MwSt)