Tag: Quebec

Issuance, Preparation, Storage, Usage and Disposal of Disinfectant Solution in Pharma Industry

February 23, 2021December 26, 2023 ABHA

Issuance, Preparation, Storage, Usage and Disposal of Disinfectant Solution in Pharma Industry Objective To lay down a procedure for issuance, preparation, storage, usage and disposal of disinfectant solution in Pharma Industry. Scope This SOP is applicable for issuance, preparation, storage, usage and disposal of disinfectant solution in manufacturing area in Pharma Industry. Responsibility GMP coordinator…

SOPs

Corrective and Preventive Action (CAPA) In Pharma Industry

February 22, 2021December 26, 2023 ABHA

Corrective and Preventive Action (CAPA) In Pharma Industry Objective To lay down a procedure for the Corrective and Preventive Action so as to eliminate the causes of potential non-conformities and /or encountered non-conformities in order to prevent their occurrence and / or recurrence In Pharma Industry. Scope This Standard Operating Procedure shall apply to all…

SOPs

Organogram in Pharma Industry

February 22, 2021December 26, 2023 ABHA

Organogram in Pharma Industry in Pharma Industry Objective To describe the procedure for preparation of Organogram in Pharma Industry. Scope This procedure is applicable for preparation of organograms of all the departments in Pharma Industry. Responsibility P&A Department is responsible for preparation of organogram. Head – User department is responsible for review of respective Organograms….

SOPs

Cleaning Policy of Area and Equipment in Pharma Industry

February 22, 2021December 26, 2023 ABHA

Cleaning Policy of Area and Equipment in Pharma Industry Objective To lay down the procedure for Cleaning Policy of Area & Equipment in Pharma Industry. Scope This Standard Operating Procedure is applicable to all the departments at the formulation plant in Pharma Industry. Responsibility Production Operator/ Technician shall be responsible for cleaning. Production &…

SOPs

Procedure for autoclave validation

February 19, 2021December 26, 2023 ABHA

STANDARD OPERATING PROCEDURE Title : Procedure for autoclave validation Department : Quality Control-Microbiology OBJECTIVE To lay down a procedure for autoclave validation. SCOPE This SOP is applicable for autoclave validation in microbiology laboratory . RESPONSIBILITY Officer / Executive-QC – responsible for Implementation of SOP. ACCOUNTABILITY Manager – Quality Control PROCEDURE…

SOPs

Procedure For Dispensing of Packing Materials

February 17, 2021February 11, 2023 ABHA

STANDARD OPERATING PROCEDURE Title : Procedure For Dispensing of Packing Materials OBJECTIVE This SOP describes the procedure for dispensing of packing material. SCOPE This procedure is applicable to Warehouse department for dispensing of packing material. RESPONSIBILITY Officer / Executive-WH – responsible for Implementation of SOP. ACCOUNTABILITY Manager-Warehouse PROCEDURE After receiving batch requisition from…

SOPs

SILDENAFIL CITRATE TABLETS

February 12, 2021July 31, 2023 ABHA

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…

MASTER FORMULAS, Tablets

Procedure For Handling of Market Complaints

February 11, 2021February 11, 2023 ABHA

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…

SOPs

Chlorzoxazone ,Nimesulide Tablet

January 25, 2021February 11, 2023 ABHA

Chlorzoxazone ,Nimesulide Tablet PURPOSE: This Master formula record (MFR) is written to describe the formulae, manufacturing procedure, specifications, packing details of dosage form. SCOPE: This MFR is performed and is applied during the manufacturing of dosage form. RESPONSIBILITY / ACCOUNTABILITY: It is the responsibility of Manufacturing Chemist to follow and adhere to this SOP. The…

Tablets

Procedure For Terminal Inspection

January 15, 2021February 11, 2023 ABHA

STANDARD OPERATING PROCEDURE Title : Procedure For Terminal Inspection Department : Quality Assurance OBJECTIVE To lay down the procedure for Terminal Inspection. SCOPE This procedure is applicable for terminal inspection and transfer of finish goods activities during processing of product. RESPONSIBILITY Officer-Production Officer-IPQA/QA ACCOUNTABILITY Manager-Production Manager-Quality Assurance PROCEDURE Terminal inspection procedure includes the verification of…

SOPs

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