CDs of Recorded Webinars

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	Time(min.)	Cost ($USA)	Topic
	62	$200	Issues in Campaigns for Cleaning Validation
	93	$200	Are We Setting Limits Correctly?
	68	$200	PAT for Cleaning Processes
	62	$200	Utilizing ICHQ7A Principles in a Risk-based Approach
	58	$200	Limits Based on Stratified Sampling
	63	$200	Impact of Degradation on Biotech Cleaning Validation
	67	$200	Implications of FDA Process Validation Guidance for Cleaning Validation Programs
	68	$200	Understanding and Improving Swabbing and Swab Recovery
	67	$200	Product Grouping for Non-Dedicated Equipment
	60	$200	Cleaning Validation for Manual Cleaning
	67	$200	Limits Based on Criteria Other than a Dose
	77	$200	Use of TOC for Cleaning Validation
	68	$200	Proper Use of Rinse Sampling
	77	$200	Bioburden and Other Microbiological Issues in Cleaning Validation
	58	$200	Cleaning Validation for Lyophilizers
	68	$200	Failure Mode Effects Analysis for Cleaning Processes
	66	$200	“Visually Clean” for Cleaning Validation
	66	$200	Streamlining Cleaning Validation
	86	$200	Using Dose-Based Limit Calculations
	72	$200	Design and Development of Cleaning Processes
	73	$200	Analytical Methods for Cleaning Validation
	51	$200	Revised System for Expressing Limits for Carryover Calculations