Dirigeants et représentants réglementaires de North-vision
1 contact identifié
TSAI Sherry
Ensuring that:
1.The conformity of medical devices is checked in accordance with the
QM system (Article 10(9)).
2.The technical documentation is kept up to date (Article 10(4) and (6)).
Market surveillance is performed in compliance with the EU
regulations (Article 10(10)).
3.The reporting obligations according to the EU regulations are met
(Article 10(13)).