Workshop: Pharmacovigilance Inspections/audits readiness and procedures to manage these
PATH & DCVMN consultant
1. Role of QPPV, staff and management
2. Training of personnel for pharmacovigilance
3. Facilities and equipment for pharmacovigilance
4. Contractual agreements
Registration link:
https://dcvmn.webex.com/dcvmn/onstage/g.php?MTID=ee5b5352e295aad1ff4d025797eb5ffdf
Event password: PVaudits2
PRE-READING MATERIAL:
https://www.ema.europa.eu/en/documents/scientific-guideline/guideline-good-pharmacovigilance-practices-module-i-pharmacovigilance-systems-their-quality-systems_en.pdf
https://www.ema.europa.eu/en/documents/scientific-guideline/guideline-good-pharmacovigilance-practices-module-ii-pharmacovigilance-system-master-file-rev-2_en.pdf
Click here to access the recording of the event
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