Pharmaceutical NEWS - Spring 2010

Newsmakers

Perspectives on Method Validation II: Validation is a multistep process with USP regulatory guidelines at each step
Pharmaceutical Formulation Quality, February/March 2010

Authors:
Heather Bridwell - Group Leader/Chemist
Jennifer Roark - Group Leader/Chemist
Thomas Lehman, PhD - Manager of Method Development

Perspectives on Method Validation: Importance of adequate method validation
Pharmaceutical Formulation Quality, December/January 2010

Authors:
Heather Bridwell - Group Leader/Chemist
Vikas Dhingra, PhD - Group Leader/Biochemist
Daniel Peckman, PhD - Group Leader/Biochemist
Jennifer Roark - Group Leader/Chemist
Thomas Lehman, PhD - Manager of Method Development

Analytical Strategies for Monitoring Residual Impurities - Best methods to monitor product-related impurities throughout the production process.
Biopharm International, January 2010

Author:
Jon S. Kauffman, PhD
Director of Biopharmaceutical Services and
Analytical Method Development / Validation

Do you have the workload but not the workforce.
Life Science Leader, January 2010

Author:
Beth DiPaolo
Managing Director
Professional Scientific Staffing