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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