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Eurofins Lancaster Labs' published articles from 2016

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Glycosylation: A Critical Quality Attribute for Biopharmaceutical Products
American Pharmaceutical Review, December 2016

Authors
Dr. Jon S Kauffman, Senior Director, Biochemistry, Method Development & Validation and Protocol Development and Technical Writing
Zsuzsa Lakos, Ph.D., Principal Scientist, Biochemistry Method Development & Validation
Elena Dremina, Ph.D., Senior Scientist, Biochemistry Method Development & Validation
John L. Snyder, Ph.D. Research Fellow/Group Leader, Biochemistry Method Development & Validation

How the biopharmaceutical industry is embracing the insourcing business model
European Pharmaceutical Review, October 2016

Author
Beth DiPaolo, MA, President, Eurofins BioPharma Product Testing PSS Insourcing Solutions

Considerations for Globalizing Combination Products
American Pharmaceutical Review, September/October 2016

Interviewee
Dr. Albrecht Poth, Scientific Director, Eurofins Medical Device Testing

Winning the Race on Biosimilars
European Biopharmaceutical Review, July, 2016, pages 54-57. © Samedan Ltd

Authors
Dr. Jon S Kauffman, Senior Director, Biochemistry, Method Development & Validation and Protocol Development and Technical Writing, Eurofins Lancaster Laboratories
Dr. Weihong Wang, Technology Development Manager, Eurofins Lancaster Laboratories
Dr. Frederic Girard, Managing Director, Eurofins Spinnovation Analytical

Under the Microscope: An Interview with Dr. Timothy S. Oostdyk
European Pharmaceutical Review, May, 2016

Interviewee:
Dr. Timothy S. Oostdyk, Group Senior Vice President of Eurofins BioPharma Product Testing

The Role of Liquid Chromatography–Mass Spectrometry in the Characterization of Therapeutic Monoclonal Antibodies
LCGC, May 2016

Authors
Robert F. Carney, M.S., Principal Scientist, Biochemistry Method Development & Validation
Elena Dremina, Ph.D., Senior Scientist, Biochemistry Method Development & Validation
John L. Snyder, Ph.D. Research Fellow/Group Leader, Biochemistry Method Development & Validation
Zsuzsa Lakos, Ph.D., Principal Scientist, Biochemistry Method Development & Validation

Quality Metrics and Best Practices for Working with Contract Labs
Pharmaceutical Technology, February, 2016

Interviewees
Art Pezzica, Senior Director, Quality Assurance
Brittany Cloud, Senior Quality Assurance Specialist