
How to Improve Cleaning Processes
Pharmaceutical Formulation Quality, June 2009
Author:
Eric A. Lingenfelter, Group Leader/Chemist
Henry L. Evans, Chemist
Wesley B. Atkins, Senior Chemist
Harolyn M. Clow
Manager , Microbiology Department – Facility Validation & Environmental Monnitoring
CRO Roundtable - The Future Of The CRO-Pharma Relationship
Life Science Leader, March 2009
Editorial comments:
Timothy Oostdyk, Ph.D.
Executive Vice President and COO, Lancaster Laboratories
A Look at the Newly Harmonized Microbial Limits Methods and Future Impact on the Industry
Contract Pharma, March 2009
Author:
Mike Yunginger
Manager , Microbiology Department - Non-Sterile Products
Clearing the Air on Residual Solvents
Pharmaceutical Technology, February 2008
Editorial comments:
Travis Emig
Director of Pharmaceutical Sciences
Delwyn Schumacher
Principal Chemist, Analytical Method Development / Validation
Outsourcing Analytical Testing
Contract Pharma, September 2007
Editorial comments:
Tim S. Oostdyk, Ph.D., COO
Lancaster Laboratories
Identification and Risk-Assessment of Extractables and Leachables
Pharmaceutical Technology Primer, January 2006
Author:
Jon S. Kauffman, Ph.D.
Director of Biopharmaceutical Services and
Analytical Method Development / Validation
Validating On-line TOC Analyzers for Real-Time Release
Pharmaceutical Manufacturing, November/December, 2006
Author:
Jon S. Kauffman, Ph.D.
Director of Biopharmaceutical Services and
Analytical Method Development / Validation
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