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An Interactive Guide to Good Documentation Practice
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Personnel Qualification and Training in GxP Environments
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Compliance Monitoring Procedures for Good Laboratory Practice : OECD 2
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Conduct of Laboratory Inspections and Study Audit : OECD 3
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Compliance of Laboratory Suppliers with GLP Principles : OECD 5
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Application of the GLP Principles to Field Studies : OECD 6
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Application of the GLP Principles to Short Term Studies : OECD 7
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Role and Responsibilities of the Study Director in GLP Studies : OECD 8
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Preparation of GLP Inspection Reports : OECD 9
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The Role and Responsibility of the Sponsor in GLP Studies: OECD 11
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Requesting & Carrying Out Inspections /Study Audits in Another Country : OECD 12
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Application of the Principles of GLP to in vitro Studies : OECD 14
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Guidance on the GLP Requirements for Peer Review of Histopathology : OECD 16
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Application of GLP Principles to Computerised Systems : OECD 17
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Relationship between the OECD Principles of GLP and ISO/IEC 17025 : OECD 18
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Management, Characterisation and Use of Test Items: OECD 19
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Guidance for Review of the GLP Status of Non-Clinical Safety Studies : OECD 20
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Possible Influence of Sponsors on Conclusions of GLP Studies : OECD 21
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GLP Data Integrity : OECD 22
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Quality Assurance and GLP : OECD 23
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