Webinar On Benchmark for Cleaning Validation

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

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1361