Audit types, including: FDA mock audit, facility, process, or study audits, can differ widely among projects; however, all marketable products must undergo multiple audits for Good Laboratory Practices (GLP) compliance at some point during the course of their life cycle. Additionally, GLP compliance may require further inspections and / or audits by an independent auditor in order to bring your organization to compliance. This GLP inspection template can help you uniformly apply mock audits in your institute while having all aspects of edits covered in this template for otimal results.
This is an MS Word/pdf template of a check list for a standard GLP inspection to be used as a starting point for preparing for and/or conducting a GLP audit. We have saved this GLP inspection template in different formats (.pdf, .docx, .dotm, .dotx, .docm, .doc, and .dot) to ensure it is compatible with all systems.
Please note that in this GLP inspection template
- The blank text place holders enclosed “_____________” indicates where a specific detail is to be inserted (replace as appropriate).
- Ensure that all placeholders are replaced with project-specific information.
- Please review this template and feel free to adapt it to your specific needs.
- The logo of the Institution must be used on this form.
- Leave the template version information in the lower left hand corner of the documents.
Using this GLP inspection template and the instructions provided will assist you to:
- Qualify a contract test facility for GLP compliance.
- Make sure your preparation of an audit for GLP compliance will be consistent with ICH guidelines.
- Help auditors or QA/QC specialists in order to include the required items in their audits.
- Verify your studies were performed in a GLP-compliant manner.
Who Can Benefit From This GLP inspection template:
This GLP inspection template is intended to assist the following in preparation of audits for GLP compliance:
- Anybody who is interested in preparation for audits for GLP compliance
- Manufacturing & Production Personnel / Managers
- Research and Development Personnel (R&D) / Managers
- Quality Assurance/ Control Personnel / Managers
- Regulatory affairs personnel / managers
- Laboratory Personnel / Managers
- Clinical trial personnel
- Project Managers
- ID: 1790
- SKU: TE-0003-MQ
- Type: Template
- Format: Template File (.docx, .dotm, .dotx, .docm, .doc, and .dot)
- Date of Last Update: Aug 01, 2017
- Price: $100.00
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