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    • Batch Record Review Checklist Template/Example1 x $4.95
    • Customer Complaint Processing1 x $39.95
    • Certificate of Analysis Package1 x $9.95
    • Guidance for Manufacturing of Biological APIs for Use in Trials1 x $59.95
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    • Laboratory Notebook Documentation Guidelines Policy1 x $39.95
    • GMP Protocols and Reports1 x $39.95
    • Gowning Requirements1 x $49.95
    • Medical Device Reporting1 x $39.95
    • Creation of Performance Qualification Protocols1 x $49.95
    • Corporate QA Audits1 x $39.95
    • Creation of Installation Qualification Protocols1 x $49.95
    • Guidance on Audit Report Confidentiality1 x $39.95
    • Creation of Standard Operating Procedures1 x $39.95
    • Creation of Forms1 x $29.95
    • Audits and Reports1 x $39.95
    • Raw Material Receipt and Disposition1 x $39.95
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  • WooCommerce My Account
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  • WooCommerce Cart20
    • Batch Record Review Checklist Template/Example1 x $4.95
    • Customer Complaint Processing1 x $39.95
    • Certificate of Analysis Package1 x $9.95
    • Guidance for Manufacturing of Biological APIs for Use in Trials1 x $59.95
    • Documentation Policy1 x $39.95
    • Laboratory Notebook Documentation Guidelines Policy1 x $39.95
    • GMP Protocols and Reports1 x $39.95
    • Gowning Requirements1 x $49.95
    • Medical Device Reporting1 x $39.95
    • Creation of Performance Qualification Protocols1 x $49.95
    • Corporate QA Audits1 x $39.95
    • Creation of Installation Qualification Protocols1 x $49.95
    • Guidance on Audit Report Confidentiality1 x $39.95
    • Creation of Standard Operating Procedures1 x $39.95
    • Creation of Forms1 x $29.95
    • Audits and Reports1 x $39.95
    • Raw Material Receipt and Disposition1 x $39.95
    • Master Batch Records and Batch Record Issuance1 x $39.95
    • Corrective and Preventative Actions (CAPA)1 x $49.95
    • Personnel Qualifications1 x $39.95
    • View Cart
      Checkout

GMP Procedures (SOPs)

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    Gowning Requirements

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    Creation of Performance Qualification Protocols

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    Creation of Installation Qualification Protocols

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    Corrective and Preventative Actions (CAPA)

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    Raw Material Receipt and Disposition

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    Post Marketing Surveillance / Recalls

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    QA Hold System

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    Vendor and Contractor Operation Qualification

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    Risk Analysis

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    Third Party Change Control Oversight

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    Corporate QA Audits

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