Compliance Trainings, Online
2015-01-28
Cleaning validation is increasingly important in preventing cross contamination and interactions between active ingredients in subsequent batches run in the same equipment. This webinar will review principles of sterilization validation and using them as a benchmark for more robust cleaning validation. Emphasis will also be placed on interrelationships with other processes and using the information gained during validation to monitor and control the cleaning process to prevent failure. Areas Covered in the Session : Sterilization process description and validation options including the kinetics of lethality (bioindicator vs bioburdens) and test methods Pre-validation activities including defining worst case challenge to the process and selecting cleaning agents Aspects to consider when writing the validation protocol Sources of process variation and basics of process control Data collection and troubleshooting Post-validation (re-validation) and change control Reporting and documentation requirements Who Will Benefit: This webinar will benefit any organization that wants to validate and improve the effectiveness of their cleaning processes. Those who will benefit include: QA Managers and Engineers Manufacturing Managers and Engineers Consultants Quality System Auditors Executives and Managers responsible for validating cleaning or sterilization processes Price Tags: Live Single Live : For One Participant $ 249 Corporate Live : For Max. 10 Participants $ 899 Recording Single REC : For One Participant - Unlimited Access for 6 Months $ 299 For more information and enquiries contact us at Compliance Trainings 5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : #416-915-4458
Email : support@compliancetrainings.com
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