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- CC for SOPs, Forms, Specifications, and Procedures
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- Customer notifications (CCs)
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- FDA application documentation
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- Filed Product Annual Report Documentation
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- AQR Building Temp-Humidity Review
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- Manage master documents (paper and electronic scans)
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- Prepare documents for scanning (batch records, reports, procedures)
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- Product Reports – Cation, Residual Solvent, EI, ect.
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- Scanning and Archival of records, reports, procedures, ect.
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- Product regulatory information
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- Customer Notifications of events (CCRs, INV & DEV)
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- Annual Starting Material Review
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- Annual Quality Summary Report
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- Create Lot Fields for MFG, PKG and forms used by QA
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- Assign & Track Events (CF, IR, INV, DEV, PDV, CAPA, CCR)
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