Tag: Brisbane

PREPARATION AND CONTROL OF BMR AND BPR IN PHARMA OBJECTIVE: To describe the procedure to be followed for preparation, and control of Batch Manufacturing Records and Batch Packing Records. SCOPE: 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: To lay down the responsibilities of the Quality Assurance Department. SCOPE: The scope of this document is to provide the responsibilities of QA . RESPONSIBILITY:  QA Personnel: To perform as per procedure. ACCOUNTABILITY: 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: To lay down a standard operating procedure for organizing and conducting Training and need gap analysis to all the employees at all levels. SCOPE: 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…

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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: Concerned Executive / Concern…

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