Medical Developments International Limited

Dispositifs placés dans 12 pays

• Autriche1
• Tchéquie1
• Danemark1
• Finlande1
• France1
• Croatie1
• Irlande1
• Islande1
• Norvège1
• Suède1
• Slovénie1
• Slovaquie1

• Ministerie van Volksgezondheid, Welzijn en Sport
  Pays-BasContacter l’autorité →

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5 contacts identifiés

• RS
  RAVI Srividhya

  PCVRR
  Voir le profil →
• YEE Sue Anne
  - Ensuring that the post-market surveillance obligations are complied with in accordance with Article 10 (10); - Ensuring that the reporting obligations referred to in Articles 87 to 91 are fulfilled; - Ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued
  Masqué
• VAISHNAV Jay
  - Ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up to date. - Ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
  Masqué
• YANEZ Patricia
  - Responsible for the control and management of all Quality activities associated with Regulatory Compliance. - Supplier Quality Assurance. - Internal audit program and inspection management for all MDI products and devices. - Specifications and Regulatory compliance. - Complaint handling. - Inspection Management - Monitor and tracking non-conformances
  Masqué
• RAVI Srividhya
  - Ensuring that the post-market surveillance obligations are complied with in accordance with Article 10 (10); - Ensuring that the reporting obligations referred to in Articles 87 to 91 are fulfilled; - Ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued
  Masqué

• MDI — AU-MF-000013818
• MDI — AU-PR-000014568
• Emergo Europe B.V. — représente — AU-MF-000013818
• RAVI Srividhya — MDI