Mark P. Mathieu

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Good Clinical Practice: A Question & Answer Reference Guide 2010

by Mark P. Mathieu First published in 2005 — 4 editions
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Global Biotechnology Product Registration: E.U., U.S., and Japan

by Mark-Michael Struck, Hiromi Okabe, and Mark P. Mathieu First published in 1997 — 2 editions

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Biologics Development: A Regulatory Overview

by Mark P. Mathieu First published in 1997 — 2 editions

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New drug development: a regulatory overview

by Mark P. Mathieu First published in 1994 — 2 editions
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New Drug Development: A Regulatory Overview

by Mark P. Mathieu and Mark Mathieu First published in 2000 — 1 edition

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PAREXEL's handbook of CDER staffing and drug review

by Mark P. Mathieu First published in 1996 — 1 edition

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New drug development: a regulatory overview

by Mark P. Mathieu and Murphy, William J. First published in 1987 — 1 edition
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Biologics development: a regulatory overview

by Mark P. Mathieu First published in 1997 — 1 edition
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Biologics development: a regulatory overview

by Mark P. Mathieu First published in 1993 — 1 edition
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Parexel's Pharmaceutical R & D Statistial Source- Book 1999

by Mark P. Mathieu First published in 2000 — 1 edition

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Parexel's Pharmaceutical R & D Statistical Sourcebook 2002/2003

by Mark P. Mathieu First published in 2002 — 1 edition

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Parexels Pharmaceutical R and d Statistical Sourcebook 2004/2005

by Mark P. Mathieu First published in 2004 — 1 edition

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Parexels Pharmaceutical R and d Statistical Sourcebook 2005/2006 (Pharmaceutical R & D Statistical Sourcebook)

by Mark P. Mathieu First published in 2005 — 1 edition

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Parexel's Pharmaceutical R&d Statistical Sourcebook, 1995

by Mark P. Mathieu First published in 1995 — 1 edition

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PAREXEL's bio/pharmaceutical R & D statistical sourcebook 2009/2010

by Mark P. Mathieu First published in 2009 — 1 edition
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OLID: OL265609A

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Created April 1, 2008
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September 4, 2008	Edited by RenameBot	fix author name
April 1, 2008	Created by an anonymous user	initial import

Mark P. Mathieu

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