RFQ/OBP386/2024/25

Efficient Batch Record Design
RFQ/OBP386/2024/25
Efficient Batch Record Design and Review Course: Regulatory Requirements Applying to Batch Record Review, Pharmaceutical Documentation & the Quality System. Course must be accredited and cover the following: Regulatory Requirements Applying to Batch Record Review, Pharmaceutical Documentation & the Quality System The Design of the Master Batch Documentation Efficiency in Batch Record Review Risk Assessment/ Management Applications within the Batch Record Process Change Controls Global regulations and expectations Regulations update and latest developments in Industry
Request for Quote
2025/01/26 15:00:00
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