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21 CFR Part 211 Subpart B: Organization and Personnel
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Pharmaceutical Microbiology
Microbiological Testing Methods
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Data Integrity (ALCOA)
Data Integrity Awareness – Data Governance
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Pharmaceutical Microbiology
Control of Microbiological Contamination in a GMP Environment
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Good Manufacturing Practices (cGMP) - Advanced
21 CFR Part 211 Subpart K – Returned and Salvaged Drug Products
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Data Integrity (ALCOA)
Data Integrity Awareness: CSV Best Practices
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Good Manufacturing Practices (cGMP) - Advanced
21 CFR Part 211 Subpart D – Equipment
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Data Integrity (ALCOA)
Data Integrity Awareness: Good Documentation Practices
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