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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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Cross-contamination Risk Assessment in Pharmaceutical Manufacturing MasterClass - EU edition
07-08 December, 2023
Current regulatory requirements to perform a structured assessment of cross-contamination risks.
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Pharma Packaging Quality Control and Serialization MasterClass - EU edition
11-12 December, 2023
The course will cover serialisation and aggregation of medicinal products
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PK/PD in Drug Discovery and Development MasterClass - EU edition
12-15 December, 2023
This comprehensive and detailed online masterclass describes the PK/PD studies from an industrial perspective to achieve a successful regulatory submission.
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