ISO/IEC 17025 Documentation Toolkit

What’s included

• Ready to use documents.
• Management procedure manual
• 40+ template documents
• Instructions to use.

12 months of unlimited email support with an expert consultant

Product Description

UCS toolkit store offers readymade documents that covers the requirements of ISO standards, the documents are ready to be used by any organization by following the instructions of use. The documents are designed and created by professional consultants.

The documents do not require any further customization or edition, it is as per the ISO standards requirements and best practices in respect of design and process.

The toolkit includes the following documents.

• ·      Management Procedures Manual.docx
• ·      Quality Manual.docx
• ·      Safety Manual.docx
• ·      CONF-POL-01.docx
• ·      IMP-POL-01.docx
• ·      QMS-POL-01.docx
• ·      Standard copy
• ·      Checklist
• ·      Training material
• ·      Internal Audit Checklist.doc
• ·      Sample Audit Report.docx
• ·      F_4.1_01_Guidelines for Operation in Laboratory.docx
• ·      F_4.1_02_NDA_Third Party.docx
• ·      F_5.3_01_Range of Lab Activities.DOC
• ·      F_5.6_02_Appointment letter_Coordinator.DOC
• ·      F_6.2_01_Competence Criteria for Laboratory Staff.docx
• ·      F_6.2_02_ML of Lab Staff.doc
• ·      F_6.2_03_Personnel Training Needs.doc
• ·      F_6.2_04_Personnel Training Plan.doc
• ·      F_6.2_05_Personnel History Cards.docx
• ·      F_6.2_06_Supervision and monitoring plan.docx
• ·      F_6.2_07_Personnel Skill Assessment Study.docx
• ·      F_6.2_08_Authorization for testing activities.doc
• ·      F_6.2_09_Authorization for Laboratory Activities.docx
• ·      F_6.3_01_Housekeeping Checklist Report.DOC
• ·      F_6.3_02_Environmental Parameters Monitoring Record.doc
• ·      F_6.4_01_Master List of Equipment.DOC
• ·      F_6.4_02_Master List of Reference Material.doc
• ·      F_6.4_03_Equipment Installation Report.doc
• ·      F_6.4_04_Equipment CIM Plan.doc
• ·      F_6.4_05_Equipment Breakdown Report.doc
• ·      F_6.4_06_Equipment History Card.doc
• ·      F_6.4_07_Equipment Intermediate Checks Register.docx
• ·      F_6.4_08_Equipment Maintenance Register.docx
• ·      F_6.6_01_List of Approved External Providers.doc
• ·      F_6.6_02_External Providers Evaluation Report.doc
• ·      F_6.6_03_Quality Plan for Externally Provided Products & Services.doc
• ·      F_7.7_07_PT_ILC Summary Report.docx
• ·      F_7.1_01_Product Matrix for Decision Rule.docx
• ·      F_7.6_01_Measurement Uncertainty Sheet.xlsx
• ·      F_7.7_01_Internal & External Quality Assurance Plan.docx
• ·      F_7.7_02_External Quality Assurance Programme.docx
• ·      F_7.7_03_Re-Testing Report.docx
• ·      F_7.7_04_Replicate Testing Report.docx
• ·      F_7.9_01_Complaint Register.doc
• ·      F_7.10_01_Nonconforming Work_CA Register.doc
• ·      F_8.6_04_Suggestion Report.doc
• ·      F_8.2_01_Master List of Documents.doc
• ·      F_8.2_02_Master List of Records.doc
• ·      F_8.2_04_Master List of National_International Standards.doc
• ·      F_8.3_01_Document Change Request Note.doc
• ·      F_8.5_01_Risk Identification and Mitigation Plan.docx
• ·      F_8.6_01_Customer Feedback Form.doc
• ·      F_8.6_02_Status of Quality Objectives and Performance Parameters.doc
• ·      F_8.6_03_Monthly Meeting Summary Report.doc
• ·      F_8.8_01_Internal Audit – Annual Plan.doc
• ·      F_8.8_02_Internal Audit Notice.doc
• ·      F_8.8_03_Internal Audit Report.doc
• ·      F_8.8_04_Non-conformity Report.doc
• ·      F_8.8_05_Audit Summary Report.doc
• ·      F_8.9_01_Management Review Meeting _Annual Plan.doc
• ·      F_8.9_02_Notice for Annual Management Review Meeting.doc
• ·      F_8.9_03_Minutes of Management Review Meeting.doc

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