PURPOSE: This MFR is written to describe the formulae, manufacturing procedure, specifications, packing details of dosage form. SCOPE: This procedure is performed and is applied during the manufacturing of dosage form. RESPONSIBILITY / ACCOUNTABILITY: It is the responsibility of Assistant Manufacturing Chemist to follow and adhere to this MFR. The Production Pharmacist, QC/QA Manager are accountable…
STANDARD OPERATING PROCEDURE Title : Procedure For Handling of Market Complaints OBJECTIVE To lay down the Procedure for Handling of Market Complaints. SCOPE This Procedure is applicable for handling of market complaints received from wholesaler, Distributor, Retailer, Customer, Physicians, Patients, field staff etc. at Pharmaceutical Company. RESPONSIBILITY It is a joint responsibility of Manager-Marketing and Manager-Quality Assurance in coordination with Quality Assurance. It is a…
STANDARD OPERATING PROCEDURE Title : Procedure For Deviation control system Department: Quality Assurance OBJECTIVE To lay down the procedure for reporting and monitoring of deviations that occur during receipt and storage of material, manufacturing process of a product, testing and release of material/product, documented procedures wherever applicable. SCOPE This Procedure is applicable to all related…
Assigning Manufacturing and Expiry date to the Finished Products Objective To lay down a procedure for assigning manufacturing and expiry date to the finished products manufactured. Scope This procedure shall be applicable to all products manufactured. Responsibility Executive / Officer Production shall be responsible for assigning manufacturing and expiry date to batch of finished product…
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