Product Category

Dealing with Out of Specification (OOS) Test Results

Excel Spreadsheet Validation in GxP Environment

Deviation Management and CAPA by Leveraging Effective Investigation

Successful Change Control Management

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

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

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

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

Quality Risk Management – A Practical Approach

Product Quality Review – A Practical Approach towards Compliance

3-Hour Virtual Seminar On Risk Based Process Validation

3-Hour Virtual Seminar On How To Prepare An Effective SOP – Workshop With Case Study

3-Hour Virtual Seminar On How To Prepare An Effective SOP – Workshop With Case Study

3-Hour Virtual Seminar On Media Fill – Avoiding And Overcoming Media Fill Failures

3-Hour Virtual Seminar On Media Fill – Avoiding And Overcoming Media Fill Failures

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