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Creation of Installation Qualification Protocols
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Management Reporting and Quality Review
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Third Party Change Control Oversight
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QA Hold System
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Master Batch Records and Batch Record Issuance
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Batch Record Review
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Personnel Qualifications
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Corporate QA Audits
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Laboratory Notebook Documentation Guidelines Policy
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Laboratory Notebook Issuance
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Gowning Requirements
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Interpretation of 21 CFR Part 11
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Deviation Reporting System
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Medical Device Reporting
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GMP Protocols and Reports
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Creation of Performance Qualification Protocols
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Creation of Standard Operating Procedures
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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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Documentation Policy
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22
Creation of Installation Qualification Protocols
1 x
$
49.95
Management Reporting and Quality Review
1 x
$
39.95
Third Party Change Control Oversight
1 x
$
39.95
Audits and Reports
1 x
$
39.95
QA Hold System
1 x
$
39.95
Master Batch Records and Batch Record Issuance
1 x
$
39.95
Batch Record Review
1 x
$
39.95
Personnel Qualifications
1 x
$
39.95
Corporate QA Audits
1 x
$
39.95
Laboratory Notebook Documentation Guidelines Policy
1 x
$
39.95
Laboratory Notebook Issuance
1 x
$
29.95
Gowning Requirements
1 x
$
49.95
Interpretation of 21 CFR Part 11
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$
59.95
Deviation Reporting System
1 x
$
39.95
Medical Device Reporting
1 x
$
39.95
GMP Protocols and Reports
1 x
$
39.95
Creation of Performance Qualification Protocols
1 x
$
49.95
Creation of Standard Operating Procedures
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$
39.95
Guidance for Manufacturing of Biological APIs for Use in Trials
1 x
$
59.95
Guidance on Audit Report Confidentiality
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$
39.95
Customer Complaint Processing
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39.95
Documentation Policy
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39.95
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Quality Assurance Disposition Process
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Quality Assurance Disposition Process
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Batch Record Review
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Creation of Logs and Logbooks
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GMP Protocols and Reports
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Creation of Standard Operating Procedures
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