| Month |
Description |
|
December 2001
|
What’s a “Dose” for Calculating Limits?
|
|
November 2001
|
Cleaned Equipment Hold Time
|
|
October 2001
|
Dirty Equipment Hold Times
|
|
September 2001
|
Handling Sampling Recovery Results
|
|
August 2001
|
Equipment Grouping Strategies for Cleaning Validation
|
|
July 2001
|
Product Grouping Strategies for Cleaning Validation
|
|
June 2001
|
Water Quality for Validated Cleaning Processes
|
|
May 2001
|
Setting “Dose” Limits without Dosing Information
|
|
April 2001
|
Cleaning for Manufacture of Clinical Trial Materials (CTMs)
|
|
March 2001
|
The New FDA Compliance Program Guidance Manual and Cleaning Validation
|
|
February 2001
|
Validation of Analytical Methods
|
|
January 2001
|
Specificity of Analytical Methods
|