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Best Practices for an Effective Cleaning Validation Program

Please note that this event is already in progress or has finished.
It might be possible to obtain information from the organiser about similar future events
[or if available notes/abstract from this meeting].

Please check out any links below - if these are not of any help then contact the organiser using the "Inquire" button below.

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Date: 21st - 22nd September, 2009

Location: Malvern, PA, USA

Summary:
Pharmaceutical - Training

Attendance will be beneficial to personnel directly involved in the development of cleaning procedures, cleaning validation programs and plans. Additionally, those responsible for cleaning validation protocols and execution activities, including validation and laboratory personnel, as well as, beginning or seasoned operational personnel who will eventually participate in such efforts, will find this course particularly useful. This includes Analytical Method Development, Quality Control and Quality Assurance personnel.

Individuals in management who interact with the above or communicate with regulatory agency inspectors to rationalize or defend cleaning validation programs will also benefit from attending this course. There are no prerequisites for attending, but a basic knowledge of general science and equipment cleaning processes is helpful.

Qualification and Calibration of Quality Control Laboratory Instrumentation and Systems



Please check with the organiser to ensure that this event will be taking place
and that it is not oversubscribed before committing to travel arrangements etc.




 

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15 minute Endotoxin Testing with Endosafe PTS from Charles River