SOP for Self-Inspection and Internal Audits Standard Operating Procedure for Self-Inspection and Internal Audits in Otic Manufacturing Unit 1) Purpose To establish a framework for conducting self-inspections and internal audits…
SOP for Vendor Qualification and Management Standard Operating Procedure for Vendor Qualification and Management in Otic Manufacturing Unit 1) Purpose To establish criteria and procedures for the qualification, selection, evaluation,…
SOP for Product Recalls Standard Operating Procedure for Product Recalls in Otic Manufacturing Unit 1) Purpose To establish procedures for initiating, managing, and completing product recalls of Otic (Ear) Dosage…
SOP for Complaint Handling Standard Operating Procedure for Complaint Handling in Otic Manufacturing Unit 1) Purpose To establish procedures for receiving, documenting, evaluating, investigating, and resolving complaints related to Otic…
SOP for Training of Personnel Standard Operating Procedure for Training of Personnel in Otic Manufacturing Unit 1) Purpose To establish procedures for training personnel involved in the manufacturing of Otic…
SOP for Stability Studies and Monitoring Standard Operating Procedure for Stability Studies and Monitoring in Otic Manufacturing Unit 1) Purpose To establish procedures for conducting stability studies and monitoring of…
SOP for Quality Control Testing and Release Standard Operating Procedure for Quality Control Testing and Release in Otic Manufacturing Unit 1) Purpose To establish procedures for conducting quality control testing…
SOP for Finished Product Release Standard Operating Procedure for Finished Product Release in Otic Manufacturing Unit 1) Purpose To establish procedures for the release of finished Otic (Ear) Dosage Forms…
SOP for Labeling and Packaging Control Standard Operating Procedure for Labeling and Packaging Control in Otic Manufacturing Unit 1) Purpose To establish procedures for controlling labeling and packaging operations in…
SOP for Deviation and Out-of-Specification (OOS) Handling Standard Operating Procedure for Deviation and Out-of-Specification (OOS) Handling in Otic Manufacturing Unit 1) Purpose To establish procedures for handling deviations and out-of-specification…