Sterilization as a Benchmark for Cleaning Validation and Control - Webinar By GlobalCompliancePanel 2012
02 Aug 2012
Webinar
Key Topics
Pre-validation activities including defining worst case challenge to the process and selecting cleaning agents
Sterilization process description and validation options including the kinetics of lethality (bioindicator vs bioburden) and test methods
Sources of process variation and basics of process control
Aspects to consider when writing the validation protocol
Post-validation (re-validation) and change control
Data collection and troubleshooting
Reporting and documentation requirements
Who should Attend
Consultants, QA and Manufacturing Managers and Engineers who are responsible for validating cleaning or sterilization processes, responsible executives and Auditors.
Past Events
Sterilization as a Benchmark for Cleaning Validation and Control - Webinar By GlobalCompliancePanel 2012 - 02 Aug 2012, Webinar (31869)
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Important
Please, check "Sterilization as a Benchmark for Cleaning Validation and Control - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Healthcare, Hospitals & Clinics, Medical device, Medical laboratories, Pharma
