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<title>Guideline on the European Drug Master File Procedure updated
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<pubDate>19 Jun 2013 12:00:00 UTC</pubDate>

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<title>Written Confirmation: Japan on the List of "Third Countries"
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<pubDate>19 Jun 2013 12:00:00 UTC</pubDate>

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<title>Answers by EMA on the Topic Bioburden
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<pubDate>19 Jun 2013 12:00:00 UTC</pubDate>

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<title>WHO Guideline on Quality Risk Management finalised
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<pubDate>19 Jun 2013 12:00:00 UTC</pubDate>

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<title>MHRA implements new Software for risk based Inspection Planning
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<pubDate>19 Jun 2013 12:00:00 UTC</pubDate>

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<title>GMP-Audits of manufacturers of active substances: Minimum Requirements on Audit Reports and Qualification of Auditors
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<pubDate>12 Jun 2013 12:00:00 UTC</pubDate>

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