is being presented by Todd Arney, Principle Consultant, with Technical & Quality Services, LLC and airs on Wednesday, September 14th, 2011. For more details or to register, please visit our site at www.fxconferences.com
This audio conference presentation provides attendees with the latest information on industry standards for cleaning and cleaning validation, as well as a discussion of the current regulatory requirements and FDA guidance on the subject. Our speaker shares his wealth of experience and insight on the impact of cleaning and cleaning validation on turnover time, and how it affects overall capacity in the operating environment. Attendees learn how to implement a robust cleaning and cleaning validation program "brick by brick" in their own facilities, including cleaning procedure design, limits and matrix approach, troubleshooting failure, and presenting validation documents to regulators.
Showing posts with label Todd Arney. Show all posts
Showing posts with label Todd Arney. Show all posts
Monday, August 22, 2011
Wednesday, July 6, 2011
Process Validation – Implementing the Finalized FDA Guidance
is being presented by Todd Arney, Principal Consultant, with Technical & Quality Services, LLC and airs on Thursday, August 4th, 2011. For more details, or to register please visit our site at www.fxconferences.com
This audio conference presentation discusses the relevant regulatory requirements and current standards for process validation, and provides attendees with insight and practical guidance on how to implement them. Our speaker draws on real-life examples and shares experience and insight on the real problems fellow industry professionals are wrestling with.
The presentation reviews the fundamental regulatory requirements for process validation, and builds upon them in successive layers with current industry standards. The takeaway for attendees is a comprehensive bottom-up plan of action that pharmaceutical professionals can follow to either establish their own validation programs or enhance the ones they already have in place.
This audio conference presentation discusses the relevant regulatory requirements and current standards for process validation, and provides attendees with insight and practical guidance on how to implement them. Our speaker draws on real-life examples and shares experience and insight on the real problems fellow industry professionals are wrestling with.
The presentation reviews the fundamental regulatory requirements for process validation, and builds upon them in successive layers with current industry standards. The takeaway for attendees is a comprehensive bottom-up plan of action that pharmaceutical professionals can follow to either establish their own validation programs or enhance the ones they already have in place.
Subscribe to:
Posts (Atom)