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| Event 1 - 10 of 81 in the category Analysis
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How to comply with recent expectations for Extractables /Leachables testing for Biologics
This Webinar will discuss the test conditions of Extractables/Leachables and also the requirements for testing extractables/Leachables.
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22 Mar 2010 Palo Alto, USA
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Overview of FDA Regulatory Compliance for Medical Devices
This course is specifically focused on the law, regulations and policies set down by the FDA for the manufacture of medical devices. It will provide each attendee ... |
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22 Mar 2010 - 23 Mar 2010 Dublin, Ireland
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analytica 2010 - 22nd International Trade Fair for Laboratory Technology, Analysis and Biotechnology
analytica 2010 will present products and innovations in the analysis, laboratory- technology and biotechnology sectors with the usual high level of quality. As ... |
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23 Mar 2010 - 26 Mar 2010 München, Germany
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Root Cause Analysis for CAPA
Upon completion of this course, participants will have gained an understanding of the basic concepts involved in Root Cause Analysis and the tools used to conduct ... |
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24 Mar 2010 - 26 Mar 2010 Dublin, Ireland
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Effective Quality Assurance Auditing for FDA Regulated Industries
The course explores the politics, psychology and all the technical aspects of auditing, including discussions of their logistics, tools, and frequency. The course ... |
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29 Mar 2010 - 30 Mar 2010 Dublin, Ireland
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The Peptide Conference 2010
A 2 day conference with top level speakers aimed at professionals engaged in therapeutic peptide development. |
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30 Mar 2010 - 31 Mar 2010 Cambridge, United Kingdom
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Project Management for Phase 1 & 2 Clinical Trials
Efficient and effective management of Phase 1 and 2 clinical trials can significantly impact the time, scope and budget for the development of a drug or device. ... |
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08 Apr 2010 - 09 Apr 2010 Dublin, Ireland
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Wyatt Technology Europe - Advanced Macromolecular Charakterisisation - Info Seminars Spring 2010
Wyatt Technology Europe, the leading manufacturer of instruments for macromolecular characterisation, cordially invites you to a series of one-day seminars (duration ... |
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12 Apr 2010 Brüssel, Belgium
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Project Management for the Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
Speed to market is the key to driving product revenue. Managing the quality of the Phase 3 and 4 activities will impact project timing and budget and have a ... |
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12 Apr 2010 - 13 Apr 2010 Dublin, Ireland
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Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
Complex processes yielding complex products such as biologics and biopharmaceuticals demand numerous, non-compendial, and sometimes complex, QC test methods to ... |
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12 Apr 2010 - 13 Apr 2010 Berlin, Germany
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