AEMCO z.e (Pvt.) Ltd.

• Agencia Española de Medicamentos y Productos Sanitarios
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• Allemagne14

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  ELAHI Zeeshan

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• ELAHI Zeeshan
  ensuring that: (a) 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; (b) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (c) the post-market surveillance obligations are complied with in accordance with Article 10(10); (d) the reporting obligations referred to in Articles 87 to 91 are fulfilled;
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• AF Pharma Service Europe SL — représente — AEMCO z.e (Pvt.) Ltd.
• ELAHI Zeeshan — AEMCO z.e (Pvt.) Ltd.