Zakłady Farmaceutyczne Polpharma SA

SRN

PL-MF-000010601

Rôle

Fabricant

Pays

Pologne

Nom de l'organisation

Zakłady Farmaceutyczne Polpharma SA

Numéro TVA UE

592-02-02-822

Registre du commerce

0000127044

Date d'enregistrement

27 juil. 2021

Adresse

19, PELPLIŃSKA 83-200 STAROGARD GDAŃSKI POLOGNE

Téléphone

+48783838970

Email

ewa.barczewska@polpharma.com

Nom

Urząd Rejestracji Produktów Leczniczych

SRN

PL-CA-014

Téléphone

+48 22 492 11 71

Email

wm@urpl.gov.pl

• BARCZEWSKA Ewa
  the technical documentation are drawn up and kept up-to-date;
  Masqué
• ŚWIĘCICKA Katarzyna
  the technical documentation are drawn up and kept up-to-date;
  Masqué
• ZACHARSKA Jolanta
  the technical documentation are drawn up and kept up-to-date;
  Masqué
• DUZOWSKA Agnieszka
  the technical documentation are drawn up and kept up-to-date;
  Masqué
• LEWANDOWSKA Magdalena
  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;
  Masqué
• HEBEL Aleksandra
  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;
  Masqué
• RESZKE Karolina
  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;
  Masqué
• KAŹMIERCZYK-GRUCA Małgorzata
  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;
  Masqué
• KONIKOWSKA-KUZIEŃKO Anna
  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 EU declaration of conformity are drawn up and kept up-to-date;
  Masqué
• SERAFIN Anna
  - the post-market surveillance obligations are complied with in accordance with Article 10(10); - in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued. - the reporting obligations referred to in Articles 87 to 91 are fulfilled
  Masqué
• TRZEMŻALSKA - WŁADYKA Anna
  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;
  Masqué
• PIETKIEWICZ Justyna
  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;
  Masqué
• FIMOWICZ Aneta
  the EU declaration of conformity are drawn up and kept up-to-date
  Masqué

Affichage de 1–2 sur 2 dispositifs.

Dispositifs placés dans 1 pays

• Pologne2

Aucun certificat enregistré pour ce fabricant.