Preparation for the Inspection of the Pharmacovigilance System
The processes of planning, performing, documenting, and follow-up of pharmacovigilance system inspections are regulated by the Good Pharmacovigilance Practices (GVP) and local regulations. These inspection processes apply mainly to marketing authorisation holders, developers of medicinal products fo...
Bewaard in:
| Hoofdauteur: | |
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| Formaat: | Boek |
| Gepubliceerd in: |
Ministry of Health of the Russian Federation, Federal State Budgetary Institution «Scientific Centre for Expert Evaluation of Medicinal Products»,
2021-10-01T00:00:00Z.
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| Onderwerpen: | |
| Online toegang: | Connect to this object online. |
| Tags: |
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Internet
Connect to this object online.3rd Floor Main Library
| Plaatsingsnummer: |
A1234.567 |
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| Kopie 1 | Beschikbaar |