URS (USER REQUIREMENT SPECIFICATION) PROTOCOL FOR WASHING MACHINE

URS (USER REQUIREMENT SPECIFICATION) PROTOCOL FOR WASHING MACHINE This is a specific document prepared for the sterile facility. Hence, this document before being effective shall be approved and authorized by Unit Head and accepted by Vendor/Supplier. List of Content Front Page Index Approval Objective Responsibility Equipment description & Identification User Requirement Complementary aspects Safety and … Read more

URS (USER REQUIREMENT SPECIFICATION) PROTOCOL FOR HPHV STEAM STERILIZER

URS (USER REQUIREMENT SPECIFICATION) PROTOCOL FOR HPHV STEAM STERILIZER This is a specific document prepared for the sterile facility. Hence, this document before being effective shall be approved and authorized by Unit Head and accepted by Vendor/Supplier. List of Content Front Page Index Approval List of general components Glossary Technical General Salient features Operational requirements … Read more

SOP on Cleaning, Maintenance and Calibration of Stability Chamber

SOP on Cleaning, Maintenance and Calibration of Stability Chamber Objective: To lay down a procedure for cleaning, maintenance and calibration of stability chamber. Scope: This SOP is applicable for the cleaning, maintenance and calibration of stability chamber. Responsibility: QC Chemist or above AND Electrician or above Accountability: Head – Quality Control & Head – Engineering Procedure: Cleaning: Chamber shall be cleaned … Read more

SOP on receipt and handling of stability samples

SOP on receipt and handling of stability samples Objective: To lay down a procedure for receipt and handling of stability samples. Scope: This SOP is applicable for receipt and handling of stability samples in Quality Control Laboratory. Responsibility: QC Chemist or above Accountability: Head – Quality Control Procedure: Receipt of stability samples : Samples for stability studies shall be … Read more

SOP on Pharmacopeial updation of documents as per the Pharmacopeial changes

SOP on Pharmacopeial updation of documents as per the Pharmacopeial changes Objective: To lay down a procedure for Pharmacopeial updation of documents as per the Pharmacopeial changes. Scope: This procedure is applicable to Pharmacopeial updation of documents as per the Pharmacopeial changes.. Responsibility: QC Chemist or above & QA officer or above Accountability: Head Quality Control & Head Quality Assurance Procedure: … Read more

SOP on Retesting of Raw Material

SOP on retesting of raw material Objective: To lay down the procedure for re-testing of raw material for material lying in warehouse for longer period. Scope: This SOP is applicable for retesting of raw material for material lying in warehouse for longer period. Responsibility: Chemist or above of QC Department & Officer or above of warehouse Department. Accountability: Head – … Read more

SOP on Sampling of Raw Material

SOP on Sampling of Raw Material Objective: To lay down the procedure for sampling of raw material. Scope: This procedure is applicable for sampling of raw material Responsibility: Chemist or above Accountability: Head – Quality Control Procedure: Sampling of Raw Materials: Raw material sampling shall be initiated after receiving the “GRN” from warehouse. Ensure that material is received from … Read more

SOP FOR INCIDENCE HANDLING

SOP FOR INCIDENCE HANDLING PURPOSE: To lay down a procedure for reporting, investigation and disposition of Incidents. SCOPE: this procedure is applicable to the reporting of investigation and disposition of unplanned, uncontrolled incidents either directly or indirectly associated with Manufacturing/Packaging, or Analytical operations. RESPONSIBILITY: Observer / Concerned Department Officer shall report the Incident. Observer / … Read more

SOP FOR HANDLING OF OUT OF CALIBRATION

SOP FOR HANDLING OF OUT OF CALIBRATION PURPOSE: To lay down a procedure for handling of out of calibration of instruments. SCOPE: This SOP is applicable for all the instruments available. RESPONSIBILITY Preparation of SOP: Officer /Sr. Officer QA Department. Checking and Review of the SOP: Officer /Executive QA Department. Approval of the SOP: Executive … Read more

CHECKLIST FOR PREVENTIVE MAINTENANCE OF COMPRESSION MACHINE

CHECKLIST FOR PREVENTIVE MAINTENANCE OF COMPRESSION MACHINE Equipment code: ___________________________ Frequency:  Quarterly Open and clean the panel internally and externally using vacuum cleaner/air blower. Visually check the tightness of cable termination at MCCB incoming and outgoing side and at outgoing MCB. Check the operation and setting of all machine interlocking. Check all terminations for overheating. … Read more