Articles by Thomas A. Little, PhD - BioPharm International

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Articles by Thomas A. Little, PhD

Essentials in Quality Risk Management
May 1, 2013
By: Thomas A. Little, PhD

Quality risk management is an essential element of every aspect of drug development and manufacturing throughout the product lifecycle.

Assay Development and Method Validation Essentials
November 1, 2012
By: Thomas A. Little, PhD

A 10-step systematic approach to analytical method development and validation can improve the quality of drug development.

Using a Systematic Approach to Select Critical Process Parameters
July 1, 2012
By: Thomas A. Little, PhD

Harmonized regulations call for a risk-based and systematic approach to evaluating and selecting CPPs.