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BMC Musculoskeletal Disorders

12/22/2009

Nicholas McArthur , Lydia Heimann , Elvira Dingeldein , Héloïse Cavey , Xavier Palazzi , Gaëlle Clermont, Franz-Xaver Huber and Jean-Pierre Boutrand
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Assessing Biological Safety of Metals Associated with Medical Devices

10/1/2009
D.E. Albert, A.M. Hoffmann, H. Sy and G.M. Ziegler
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Biological Safety: More Than Just Test Data

1/1/2009
David Parente
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Assessing the Biological Safety of Polymers

9/1/2008
David Albert and Amy Hoffmann
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Using Chemical Characterization to Show Equivalency

5/1/2008
David Albert PhD and Amy Hoffmann
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Evaluating Pharmaceutical Container Closure Systems

1/1/2008
Dr. David E. Albert
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Antimicrobial Efficacy Comparison of Floor Coverings

1/1/2008
Beth Joiner
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Progress in Testing

1/1/2008
Dr. Paul J. Upman
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The Growing Importance of Materials Characterization in Biocompatibility Testing

1/1/2008
Dr. David Albert
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Biological Indicator Characterization

3/29/2007
Joel R. Gorski, PhD
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Making Sure It's Sterile

7/1/2006
John Broad and Laurie Nawrocki
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The Challenge to Global Acceptance of Part 3 of ISO 10993

6/1/2006
Dr. Joseph Carraway and Dr. Molly Ghosh
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ISO 10993-6: Tests for Local Effects After Implantation

4/1/2006
Paul J. Upman, Ph.D.
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Avoiding Loss of Medical Information During Clinical Investigations

5/1/2005
Raphael Gruber
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The Expanding Role of Contract Research Organizations

4/1/2005
Dr. Paul Upman and Terry Langenderfer
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When To Conduct A Clinical Trial

10/1/2004
J.P. Boutrand
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The Important Role Of Material And Chemical Characterisation In Device Evaluation

8/1/2004
David E. Albert
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Outsourcing Testing Services

7/20/2004
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The Growing Importance of Materials Characterization in Biocompatibility Testing

3/1/2002
Dr. David E. Albert
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Current and Future Issues in Sensitization Testing

9/1/2001
R. Eloy, F. Charton-Picard, C. Delubac and S. Kergozien
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Progress in Testing

9/1/2001
Paul J. Upman, NAMSA
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BIOMATECH NAMSA Testing Laboratory Prevention of bacterial adhesion to medical polymers

9/1/2001
Docteur Sophie BOBIN-DUBREUX
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Current and Future Issues in Sensitisation Testing

9/1/2001
R. Eloy, F.Charton-Picard, C. Delubac and S.Kergozien
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A Practical Guide to ISO 10993-3: Carcinogenicity

1/1/1999
Paul J. Upman and Richard F. Wallin
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A Practical Guide to ISO 10993-12: Sample Preparation and Reference Materials

12/1/1998
Timothy Jansen and Richard F. Wallin
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A Practical Guide to ISO 10993-4: Hemocompatibility

11/1/1998
J. Matthew Buchanan, Paul J. Upman, and Richard F. Wallin
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A Practical Guide to ISO 10993-3: Genotoxicity

10/1/1998
Gina M. Johnson, Paul J. Upman, and Richard F. Wallin
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A Practical Guide to ISO 10993-11: Designing Subchronic and Chronic Systemic Toxicity Tests

9/1/1998
Louis E. Sendelbach and Richard F. Wallin
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A Practical Guide to ISO 10993-6: Implant Effects

8/1/1998
Richard F. Wallin and Paul J. Upman
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A Practical Guide to ISO 10993-11: Systemic Effects

7/1/1998
Richard F. Wallin and Paul J. Upman
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A Practical Guide to ISO 10993-10: Irritation

6/1/1998
Richard F. Wallin and Paul J. Upman
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A Practical Guide to ISO 10993-10: Sensitization

5/1/1998
Richard F. Wallin and Paul J. Upman
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A Practical Guide to ISO 10993-5: Cytotoxicity

4/1/1998
Richard F. Wallin and Edward F. Arscott
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A Practical Guide to ISO 10993-14: Materials Characterization

2/1/1998
David E. Albert and Richard F. Wallin
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A Practical Guide to ISO 10993: Part 1 - Introduction to the Standards

1/1/1998
Richard F. Wallin and Paul J. Upman
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Validating Reusable Medical Devices: An Overview

1/1/1996
Susanne Anderson, Ed Arscott, John Broad, and Dave Parente
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Satisfying Medical Device Biocompatibility Requirements: What's a Supplier to Do?

1/1/1996
Paul J. Upman, NAMSA, Inc. & Robert Charton, Norton Performance Plastics
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