Officers and regulatory representatives of Allergan
GIACOMINI Annie
In the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
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TEYROUZ Emilien
- The conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released,
- the post-market surveillance obligations are complied with in accordance with Article 10 (10),
- the reporting obligations referred to in Articles 87 to 91 are fulfilled.
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PERRIN Véronique
The technical documentation and EU declaration of conformity are drawn-up and kept up-to-date,