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Company A produces liquid Product A and Product B and crystalline Product B which are sold asUSP grade products. Therefore, the purpose of the audit was to ascertain the degree of complianceto International Pharmaceutical Excipient Council (IPEC:PQG) Good Manufacturing Practices forPharmaceutical Excipients in the manufacture, handling, storage and testing of these products. Thescope of the audit encompassed raw material receipt to initial finished product distribution at acontracted off-site warehouse owned and operated by Warehouse Company X. The assessmentincluded review of procedures, records, and quality control systems established for theseoperations. This summary indicates the auditor’s judgment as to the extent of Company A’scompliance with the guidance set forth in the IPEC:PQG GMPs and opportunities for improvement.
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