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2-Day Hybrid Seminar on cGMP for QC Labs

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2-Day Hybrid Seminar on Root Cause Analysis & CAPA

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1-Day Hybrid Seminar on Computer System Validation Masterclass

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1-Day Hybrid Seminar on Cleaning Validation Modern Techniques, Application And Controls

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6-Hour Virtual Seminar on QbD and Technology Transfer Program – A Practical Approach to

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6-Hour Virtual Seminar on Annual Product Quality Reviews – Preparation, Reports, Impact

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The Annual Validation Summit – 2021

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Dealing with Out of Specification (OOS) Test Results

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Excel Spreadsheet Validation in GxP Environment

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Deviation Management and CAPA by Leveraging Effective Investigation

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Successful Change Control Management

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Use of Statistical Process Control and Process Capability in Line with FDA Expectations

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IQ, OQ, PQ and Validation of Laboratory Equipments and Systems

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Root Cause Analysis and CAPA with Real-Time Case Studies – 3-Hour Virtual Seminar

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cGMP as per 21 CFR 210 and 211, and Controls during Pandemic – 3-Hour Virtual Semina

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