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MD-Pharm has established and maintains own pharmacovigilance system. The company was successfully audited by the local State Authority. Our service covers the following areas:

  • Creation or revision of the pharmacovigilance system of customers
  • Receipt and processing of the reports of adverse reaction - Individual Case Safety Reports (ICSR), follow-up
  • Preparation and submission of PSURs according to GVP
  • Service of Qualified Person for Pharmacovigilance (QPPV)
  • Risk management system


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    MD-Pharm Ltd., L. Horke 15/66, 747 21 Kravare, Czech Republic
    Phone: +420 553 671 756, +420 553 671 746, Fax: +420 553 671 746
    E-mail: md-pharm@md-pharm.cz

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