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Management Reporting and Quality Review
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Laboratory Notebook Documentation Guidelines Policy
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Deviation Reporting System
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Creation of Operational Qualification Protocols
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49.95
Creation of Performance Qualification Protocols
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49.95
Creation of Standard Operating Procedures
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39.95
Gowning Requirements
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49.95
QA Hold System
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39.95
GMP Protocols and Reports
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39.95
Risk Analysis
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39.95
Post Marketing Surveillance / Recalls
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39.95
Creation of Installation Qualification Protocols
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49.95
Customer Complaint Processing
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39.95
Medical Device Reporting
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Guidance for Manufacturing of Biological APIs for Use in Trials
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16
Management Reporting and Quality Review
1 x
$
39.95
Laboratory Notebook Documentation Guidelines Policy
1 x
$
39.95
Deviation Reporting System
1 x
$
39.95
Vendor and Contractor Operation Qualification
1 x
$
39.95
Creation of Operational Qualification Protocols
1 x
$
49.95
Creation of Performance Qualification Protocols
1 x
$
49.95
Creation of Standard Operating Procedures
1 x
$
39.95
Gowning Requirements
1 x
$
49.95
QA Hold System
1 x
$
39.95
GMP Protocols and Reports
1 x
$
39.95
Risk Analysis
1 x
$
39.95
Post Marketing Surveillance / Recalls
1 x
$
39.95
Creation of Installation Qualification Protocols
1 x
$
49.95
Customer Complaint Processing
1 x
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39.95
Medical Device Reporting
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39.95
Guidance for Manufacturing of Biological APIs for Use in Trials
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59.95
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Audits and Reports
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Audits and Reports
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Batch Record Review
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Batch Record Review
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Batch Record Review Checklist Template/Example
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Batch Record Review Checklist Template/Example
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Certificate of Analysis Package
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Certificate of Analysis Package
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Corporate QA Audits
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Corporate QA Audits
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Corrective and Preventative Actions (CAPA)
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Corrective and Preventative Actions (CAPA)
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Creation of Forms
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Creation of Forms
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Creation of Installation Qualification Protocols
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Creation of Item Specifications
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Creation of Item Specifications
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Creation of List Documents
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Creation of List Documents
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Creation of Logs and Logbooks
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Creation of Logs and Logbooks
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Creation of Operational Qualification Protocols
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Creation of Performance Qualification Protocols
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Creation of Standard Operating Procedures
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Customer Complaint Processing
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Deviation Reporting System
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Document Change Control
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Document Change Control
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Documentation Policy
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Documentation Policy
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GMP Protocols and Reports
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Gowning Requirements
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Guidance for Manufacturing of Biological APIs for Use in Trials
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Guidance on Audit Report Confidentiality
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Guidance on Audit Report Confidentiality
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Interpretation of 21 CFR Part 11
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Interpretation of 21 CFR Part 11
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Laboratory Notebook Documentation Guidelines Policy
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Laboratory Notebook Issuance
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Laboratory Notebook Issuance
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Management Reporting and Quality Review
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Master Batch Records and Batch Record Issuance
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Master Batch Records and Batch Record Issuance
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Medical Device Reporting
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Personnel Qualifications
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Personnel Qualifications
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Pest Control Policy
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Pest Control Policy
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Post Marketing Surveillance / Recalls
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QA Hold System
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Quality Assurance Disposition Process
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Quality Assurance Disposition Process
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Raw Material Receipt and Disposition
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Raw Material Receipt and Disposition
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Reagent and Powder Filling / Labeling Procedure
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Reagent and Powder Filling / Labeling Procedure
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19.95
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Regulatory Inspections
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