Investigation Reports INVESTIGATION REPORT DUST GENERATION DURING COMPRESSION STAGE INVESTIGATION REPORT Dust Generation During Compression Stage Investigation Details Company Name: XXYYZZ Company… PharmaGuide HubOctober 17, 2026No comments
Investigation Reports INVESTIGATION REPORT BATCH MIXING ERROR OBSERVED DURING INSPECTION AFTER COMPRESSION NVESTIGATION REPORT Batch Mixing Error Observed During Inspection After Compression Investigation Details… PharmaGuide HubOctober 16, 2026No comments
Investigation Reports INVESTIGATION REPORT CAPSULE SHELL SOFTENING DUE TO HIGH HUMIDITY INVESTIGATION REPORT Capsule Shell Softening Due to High Humidity During Pharmaceutical Manufacturing… PharmaGuide HubOctober 15, 2026No comments
Investigation Reports INVESTIGATION REPORT BATCH MIXING ERROR OBSERVED DURING INSPECTION AFTER COMPRESSION NVESTIGATION REPORT BATCH MIXING ERROR OBSERVED DURING INSPECTION AFTER COMPRESSION INVESTIGATION REPORT Batch… PharmaGuide HubOctober 14, 2026No comments
Investigation Reports INVESTIGATION REPORT FOR MOISTURE CONTENT AFTER DRYING OUTSIDE SPECIFIED LIMIT INVESTIGATION REPORT Observation: Moisture Content After Drying Outside Specified Limit Company Name: XXYYZZ… PharmaGuide HubOctober 9, 2026No comments
Investigation Reports INVESTIGATION REPORT FOR BLEND UNIFORMITY TESTING NOT PERFORMED AFTER BLENDING INVESTIGATION REPORT Observation: Blend Uniformity Testing Not Performed After Blending Company Name: XXYYZZ… PharmaGuide HubOctober 8, 2026No comments
Audit Compliance Quality Assurance (QA SOP) AUDIT COMPLIANCE REPORT FOR UNAUTHORIZED CORRECTIONS IN BATCH RECORDS AUDIT COMPLIANCE REPORT FOR UNAUTHORIZED CORRECTIONS IN BATCH RECORDS 1. Context of Observation During the WHO… PharmaGuide HubJuly 23, 2026No comments
Investigation Reports Quality Assurance (QA SOP) INVESTIGATION REPORT FOR RELATIVE HUMIDITY (RH) WAS NOT CONSISTENTLY MAINTAINED INVESTIGATION REPORT FOR RELATIVE HUMIDITY (RH) WAS NOT CONSISTENTLY MAINTAINED Background During the WHO GMP… PharmaGuide HubJuly 22, 2026No comments
Audit Compliance Quality Assurance (QA SOP) AUDIT COMPLIANCE REPORT FOR MISSING CRITICAL PROCESS PARAMETER RECORDS AUDIT COMPLIANCE REPORT FOR MISSING CRITICAL PROCESS PARAMETER RECORDS 1. Context of Observation During the WHO… PharmaGuide HubJuly 21, 2026No comments
Audit Compliance Quality Assurance (QA SOP) AUDIT COMPLIANCE REPORT FOR DELAYED RECORDING OF IN-PROCESS DATA AUDIT COMPLIANCE REPORT FOR DELAYED RECORDING OF IN-PROCESS DATA 1. Context of Observation During the WHO GMP… PharmaGuide HubJuly 20, 2026No comments