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      Courses #Quality


      QUALITY BY DESIGN (QBD) IN PHARMACEUTICAL AND MEDICAL DEVICE MANUFACTURING

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      Quality in Technology Transfer Projects

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      How to use Quality Systems Inspection Technique (QSIT) to Your Advantage

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      Quality Risk Management Overview

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      Writing Followable Procedures – Avoid Procedure Related Deviations

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      Layered Process Audits for USFDA Regulated Industries

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      Artificial Intelligence in Pharmaceutical GMP Operations - Case Studies

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      How to go Paperless in an FDA-Regulated Environment using Electronic Workflow Signature Approvals and Electronic Records

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      OBJECTIONABLE MICROORGANISMS IN BIOPHARMACEUTICAL PRODUCTION – IDENTIFICATION AND RISK MITIGATION

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      Data Integrity and Privacy – compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR

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      Step-by-Step approach for Setting up FDA Audit Ready Quality Management System (QMS) – Case Studies based training

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      Using Metrics to Monitor and Improve Your Quality System

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