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Description
- Execution and reporting GAP assessments–including CSV, process validation, and QMS requirements
- Preparation and execution of QMS audits–including critical suppliers
Order Info
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Compliance
CFR Title 21, Parts 11, 210, 211, 820 / EU GMP Annex 1, 4, 11
Specifications
Specifications
| Product Type | Controlled Environments Services |
| Federal Regulation | FDA 21 CFR |
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