SOP ON DRAIN POINT MONITORING PURPOSE: To provide a procedure for Drain Point Monitoring. SCOPE: This procedure is applicable for Drain Point Monitoring in the microbiology Lab. ATTACHMENTS : Drain Point Monitoring Schedule (Template) Drain Point Monitoring Record Intimation For Results Exceed Drain Point Monitoring Trend (Template) Annual Trend Summary Report (Template) RESPONSIBILITY: Microbiologists Person…
SOP ON HANDLING OF BIOHAZARDOUS MATERIAL IN MICROBIOLOGY LAB PURPOSE: To outline the procedure for Handling Biohazardous Material in the microbiology Lab. SCOPE: This procedure is applicable for Handling Biohazardous Material in Microbiology Lab. REFERENCES: In-House & Â ISO 45001:2018 CROSS-REFERENCE DOCUMENTS Preparation, Review, Approval, Issuance & Retrieval of Standard Operating Procedures (SOPs) Change Control Management…
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SOP ON FOGGING IN MICROBIOLOGY LAB PURPOSE: To provide a procedure for Fogging in the Microbiology Lab. SCOPE: This procedure is applicable for Fogging in the Microbiology Lab. CROSS-REFERENCE DOCUMENTS: Entry and Exit procedure in microbiology Lab. ATTACHMENTS Fogging Solution Preparation and Usage Record Fogging Agent Receiving & Consumption Record Intimation For AHU On/Off DEFINITIONS…
ENTRY AND EXIT PROCEDURE IN MICROBIOLOGY LAB PURPOSE: To provide a procedure for Entry & Exit in Microbiology Lab. SCOPE: This procedure is applicable for Entry & Exit in the Microbiology Lab. REFERENCES: In–house CROSS-REFERENCE DOCUMENTS Preparation, Review, Approval, Issuance & Retrieval of Standard Operating Procedures (SOPs) Document(S) and Data Control Procedure Attachment/Annexures/Formats Pictorial Display…
PREPARATION AND CONTROL OF BMR AND BPR IN PHARMA OBJECTIVE:Â To describe the procedure to be followed for preparation, and control of Batch Manufacturing Records and Batch Packing Records. SCOPE:Â This procedure is applicable to Preparation of BMR and BPR . RESPONSIBILITY: Production Personnel: – BMR and BPR shall be prepared by Production personnel. QA Personnel: –…
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RESPONSIBILITIES OF THE QUALITY ASSURANCE DEPARTMENT OBJECTIVE:Â To lay down the responsibilities of the Quality Assurance Department. SCOPE:Â The scope of this document is to provide the responsibilities of QA . RESPONSIBILITY:Â Â QA Personnel: To perform as per procedure. ACCOUNTABILITY:Â Head – QA. PROCEDURE: Responsibilities and procedure applicable to QA shall be in writing and same shall be followed….
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TRAINING PROCEDURE FOR PLANT PERSONNEL IN PHARMA OBJECTIVE:Â To lay down a standard operating procedure for organizing and conducting Training and need gap analysis to all the employees at all levels. SCOPE:Â This SOP is applicable for organizing and conducting Training Calendar, Programmes, Schedules, Tests to do need gap analysis of all the employees at all levels….
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DOCUMENT AND DATA CONTROL IN PHARMA OBJECTIVE: The purpose of this Standard Operating Procedure (SOP) is to lay down a procedure for issuance, Retrieval and destruction of various documents to ensure that correct versions of document are in use. SCOPE: This SOP is applicable for issuance, distribution, retrieval and destruction of Standard Operating Procedures, Master…
PREPARATION OF SOP OBJECTIVE: To lay down a standard operating procedure for preparation, approval, control, issuance, implementation, review, change and destruction of Standard Operating Procedures and Master Documents. SCOPE: This SOP is applicable for the preparation, approval, control, issuance, implementation, review, change and destruction of Standard Operating procedures in all departments. RESPONSIBILITY:Â Concerned Executive / Concern…
