AddressFacility visits to monitor the manufacturing & QC activities and ensure the compliance of system.
Handling of document management system which includes issuance, control, retrieval and archival of documents.
Review of Batch manufacturing record and Batch packing record.
Review of analytical & microbiological testing report.
Preparation and maintenance of master list for SOP, STP, SPEC, equipment & instruments.
Handling of quality Management System (Deviation, change control, OOS, OOT, CAPA, Risk management)
Make sure that codes are assigned correctly
Complying with medical coding guidelines and policies
Receiving and reviewing patients charts and documents for verification and accuracy
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