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LOG FORM: EU-QPPV Availability Test

LOG FORM: EU-QPPV Availability Test

189,00€Preis
exkl. MwSt.

This log form template is used to document periodic tests verifying that the EU-QPPV contact and availability procedure functions as intended.

 

Regular availability testing helps ensure that the EU Qualified Person for Pharmacovigilance (EU-QPPV) can be contacted as required and that the established contact procedure through the call center operates correctly.

 

The log form provides a simple structure for recording:

  • Date of the availability test

  • Confirmation that the call center was contacted successfully

  • Confirmation that the EU-QPPV was reachable

  • Outcome of the test

  • Comments or observations

  • Approval by the person performing the test

 

This documentation supports compliance with EU Good Pharmacovigilance Practice (GVP) requirements for continuous EU-QPPV availability.

OZQA_Log form_EU-QPPV Availabil…

 

Typical use cases

  • Documenting EU-QPPV availability testing

  • Supporting EU GVP compliance

  • Maintaining inspection-ready pharmacovigilance documentation

  • Verifying operational PV contact procedures

 

Document format

Editable template provided in Word format, allowing easy adaptation to the company’s pharmacovigilance procedures.

 

  • If you prefer expert guidance, OZQA provide PV Services, such as:

    • Establishment of full PV system, including PSMF and PV SOPs
    • Gap analysis of existing PV system
    • PV audits
    • QPPV support, including management of PV Agreements, PV intelligence, PV SOPs, PV training and PV compliance
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