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Pharmacovigilance Audits & Types of PV Audits
2021-10-13
The audit in the sense a systematic and independent examination of activities to identify whether the evaluated activities were performed according to decided requirements.
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Setting Drug Product Specification MasterClass - US edition
06-08 October, 2025
Bridging Science, Compliance, and Patient Safety
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Setting Drug Product Specification MasterClass - EU edition
06-08 October, 2025
Bridging Science, Compliance, and Patient Safety
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Risk based Quality management in Clinical Trials MasterClass - EU edition
14-15 October, 2025
RBQM principles that align with regulatory expectations
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