On Demand Webinar

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

Product Quality Review – A Practical Approach towards Compliance

  • 2 Hours

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

  • 3 Hours
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Medical Device QMS and Software Validation Workshop

  • 7 Hours (2 Days)

Validation of Excel Spreadsheets in GxP Environment

  • 2 Hours

3-Hour Virtual Seminar On Risk Based Process Validation

  • 3 Hours

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

  • 3 Hours

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

  • 3 Hours

Data Integrity in times of a Pandemic

  • 2 Hours

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

  • 3 Hours
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