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GMP Training
Train on 21 CFR 210, 211 and on differences to 820 at worldwide sites. Audit device manufacturing sites to determine readiness for compliance to 21 CFR Part 210, 211 for large needle and syringe device manufacturer. |
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Prepared and delivered Training Presentations on 21 CFR Parts 210, 211. Provide 210, 211 Compliance Readiness report. |
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