Navitas Networks Webinar Series on ICH E6 GCP Compliance

1st webinar of the series: Impact of ICH E6 Addendum on Quality for Sponsors (or Quality by Design in Clinical development)

Please fill the registration form to reserve your slot for all three webinars of the series

Agenda for the 1st webinar:

  • What is Quality by Design?
    • Regulatory perspective
    • Drivers for quality in the pharmaceutical industry 
  • What can we learn about Quality by design from the manufacturing industry?
    • The importance of design, control and improve.
    • Application at the project and trial level
  • Applying Quality by Design learning in manufacturing to clinical trial management
    • Risk assessments
    • Quality tolerance limits
    • Continuous process improvement
2nd Webinar - Introducing Risk Based Monitoring to your Clinical Trial
Date & Time - September 19th, 2017, Time - 15:30 UK /16:30 CET, 10:30 EST/  7:30 PST, 20:00 IS 
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3rd Webinar - How to undertake a Gap Analysis on your systems against the ICH E6 Addendum 
Date & Time - October 24th, 2017, Time - 
15:30 UK /16:30 CET, 10:30 EST/  7:30 PST, 20:00 IST
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Please fill the form to Register!

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