On Demand Webinar

2-Day Hybrid Seminar on cGMP for QC Labs

  • 2 Days

2-Day Hybrid Seminar on Root Cause Analysis & CAPA

  • 2 Days

1-Day Hybrid Seminar on Computer System Validation Masterclass

  • 1 Day

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

  • 3 Hours

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

  • 6 Hours

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

  • 6 Hours

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

  • 6 Hours

Successful Change Control Management

  • 90 Minutes

Excel Spreadsheet Validation in GxP Environment

  • 2 Hours

Dealing with Out of Specification (OOS) Test Results

  • 90 Minutes

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

  • 2 Hours

Deviation Management and CAPA by Leveraging Effective Investigation

  • 90 Minutes

Quality Risk Management – A Practical Approach

  • 2 Hours

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

  • 90 Minutes

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

  • 3 Hours
1 2 3