How to transfer QC procedures for commercial products in pharma industry - ICH and USP guidelines 2011
03 Feb 2011
Webinar
It is critical that a robust transfer program be put into place in order to head off issues. Unearthing issues at the drug development stage, rather than during routine manufacture, will improve the overall success of the project. Attend this webinar to understand the ICH and USP guidance for validation, and how to apply ICH guidelines for method transfer and how to establish boundaries.
Areas Covered in the Seminar:
ICH guidelines for validation.
USP guidelines for validation and verification.
Applications of the ICH guidelines for method transfer.
Debated topics and approaches.
Complex procedures.
Establishing boundaries.
Who Will Benefit:
This webinar will provide valuable assistance to all personnel in:
QC functions in general
QC technical transfer groups
QC validation groups
Commercial testing facilities
Product development
Commercial project support
Past Events
How to transfer QC procedures for commercial products in pharma industry - ICH and USP guidelines 2011 - 03 Feb 2011, Webinar (11849)
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Important
Please, check "How to transfer QC procedures for commercial products in pharma industry - ICH and USP guidelines" official website for possible changes, before making any traveling arrangements
