Conference
PAT and Quality by Design
Management · Quality Assurance
Key numbers
- Editions on record
- 1first in 2014
About PAT and Quality by Design
With QbD becoming a normal integrated part of most companies these days, it is important not to be left behind. Understanding regulatory requirements, PAT data and what will drive companies to have a cost efficient QbD process are all key. Yet still companies are struggling to have a fully implemented QbD system in place.
Join Thought Leaders At The 11th Annual Conference To Enable You To:
- Understand how to prepare a successful QbD submission with regulatory expertise from FDA’s Lawrence Yu and ex-EMEA’s John Purves
- Implement QbD in your company: find out how this has been done by experts in Merck, Teva and Bristol Myers Squibb
- Overcome the problems with implementing QbD in biologics: hear how this has been done in Lonza
- Implement continuous manufacturing with practical advice from the latest pilot plants from Novartis and GlaxoSmithKline
- Understand how the generics industry has complied with the mandatory QbD regulations and the benefits of this within Teva
2014’s Expert Speakers include:
Inna Ben-anat,Pedro Hernandez,Mingzhong Li,Gawayne Mahboubian-Jones,Julian Morris,Alain Poncin,Sushill Srivastava and many more...
From our listing of this edition. Details may have changed since.
Editions
| Year | Dates | Where | Exhibitors | Visitors |
|---|---|---|---|---|
| 2014 | 25–26 Mar 2014 | — | — |
Past editions from the bvents archive (2008–2019) and organiser figures where they were published.
Questions
When is PAT and Quality by Design?
The next dates haven't been confirmed. The last edition we have on record was 25–26 Mar 2014.