• Considerations When Determining a Routine Sample Size for a Retest Procedure
• An Alternative to the ESD Approach for Determining Sample Size and Test for Out-of-Specification Situations
• Use of the Bergum Method and MS Excel to Determine the Probability of Passing the USP Content Uniformity Test
• The Square Root of N Plus One Sampling Rule: How Much Confidence Do We Have?
• Stable Isotopic Characterization of Analgesic Drugs

• Implications of Photostability on the Manufacturing, Packaging, Storage, and Testing of Formulated Pharmaceutical Products
• Analytical Methods Validation: In-Process Control Methods for the manufacture of Active Pharmaceutical Ingredients
• Analytical method Equivalency An Acceptable Analytical Practice
• Frequency Modulation Spectroscopy A Novel Nondestructive Approach for Measuring Moisture Activity in Pharmaceutical Samples
• Using the Bergum Method and MS Excel to Determine The Probability of Passing the USP Dissolution Test

• Verification Methods for 198 Common Raw Materials Using a Handheld Raman Spectrometer
• Quality by Design in Freeze-Drying
• Illuminating Heavy Metals Testing
• Good Distribution Practices for Pharmaceutical Excipients
• Reference-Standard Material Qualification

These guides, like all our products, were designed with you, our customers, in mind.  Analytical Testing Vols I, II and III are packed with ideas, solutions, advice and useful information.  Use them to help you manage your business, educate your employees, and stay current on industry practices.