PROCEDURE FOR OPERATION OF UNIT DOSAGE SAMPLER

PROCEDURE FOR OPERATION OF UNIT DOSAGE SAMPLER 1.0  OBJECTIVE :  To lay down the procedure for operation and cleaning of unit dose sampler. 2.0  SCOPE :  This SOP shall be applicable for IPQA area in Quality Assurance. 3.0  RESPONSIBILITY : In process Quality Assurance Executive /Officer 4.0  ACCOUNTABILITY : Head Quality Assurance 5.0  PROCEDURE FOR OPERATING … Read more

SAMPLING OF PACKING MATERIALS

SAMPLING OF PACKING MATERIALS 1.0  OBJECTIVE : To lay down a procedure for sampling of packaging materials. 2.0  SCOPE : To describe the procedure for sampling of Primary packing materials i.e. Aluminium Foil, Blister Aluminium Foil, PVC Film etc. and secondary packing materials i.e. Cartons, labels, Leaflet shipper etc. 3.0  RESPONSIBILITY :Quality Control Executive/Officer 4.0 ACCOUNTABILITY : Quality … Read more

PROCEDURE FOR CLEANING AND STORAGE OF SAMPLING DEVICES.

PROCEDURE FOR CLEANING AND STORAGE OF SAMPLING DEVICES. OBJECTIVE :  To lay down the procedure for Cleaning and storage of sampling devices. SCOPE :  This SOP shall be applicable for  Cleaning of all type of Sampling devices. RESPONSIBILITY : Quality Control Technician ACCOUNTABILITY :Executive / Officer – Quality Control PROCEDURE After the sampling, keep the sampling … Read more

SAMPLING OF RAW MATERIALS

SAMPLING OF RAW MATERIALS 1.0 OBJECTIVE : To lay down a procedure for sampling of Raw Materials so as to get a representative sample of the whole lot for analysis. 2.0 SCOPE : This SOP shall be applicable to sampling of all Raw materials. 3.0 RESPONSIBILITY : Quality Control Executive/Officer 4.0 ACCOUNTABILITY : Head Quality Assurance … Read more

PROCEDURE FOR VIABLE AIR MONITORING

PROCEDURE FOR VIABLE AIR MONITORING 1.0 OBJECTIVE : To lay down a procedure for environmental monitoring of air. 2.0  SCOPE : This SOP shall provide the procedure for monitoring the viable air borne count in unit II. 3.0  RESPONSIBILITY  : Quality Control Executive / Officer. 4.0  ACCOUNTABILITY : Head Quality Assurance. 5.0 PROCEDURE  The microbial environmental conditions of … Read more

PROCEDURE FOR MICROBIOLOGICAL MONITORING OF WATER

PROCEDURE FOR MICROBIOLOGICAL MONITORING OF WATER 1.0 OBJECTIVE : To lay down a procedure for microbiological monitoring of raw water and purified water. 2.0 SCOPE :This SOP shall provide the procedure for sampling and testing of raw water, soft water and purified water from all the user points and all the points across the critical functions … Read more

INPROCESS CONTROL OF PACKING LINE

IN-PROCESS CONTROL OF PACKING LINE 1.0   OBJECTIVE : To ensure quality of Finished Products during strip packing and final packing operation of tablets. 2.0 SCOPE:  This SOP shall be applicable in-process controls during strip packing and final packing operation of tablets. 3.0  RESPONSIBILITY In process Quality Assurance Officer / Executive. 4.0   ACCOUNTABILITY : Head Quality Assurance 5.0  … Read more

SAMPLING OF INTERMEDIATES AND FINISHED PRODUCTS

SAMPLING OF INTERMEDIATES AND FINISHED PRODUCTS 1.0  OBJECTIVE : To lay down a procedure for sampling of intermediate(blend/core/coated/capsules) and finished products (packing)during manufacturing operations. 2..0  SCOPE : This SOP shall be applicable to the IPQA in Quality Assurance Department. 3.0    RESPONSIBILITY : In process Quality Assurance Executive/Officer 4.0    ACCOUNTABILITY :  Head Quality Assurance 5.0    … Read more

INPROCESS CONTROL DURING TABLET MANUFACTURING

IN-PROCESS CONTROL DURING TABLET MANUFACTURING 1.0  OBJECTIVE :To lay down the procedure for In process Controls during Tablet   Manufacturing. 2.0 SCOPE :This SOP shall be applicable for in process controls during tablets manufacturing/ This SOP shall be applicable to IPQA in Quality Assurance Department. 3.0 RESPONSIBILITY In process Quality Assurance Executive/Officer.  4.0 ACCOUNTABILITY Head Quality … Read more

PROCEDURE FOR LINE CLEARANCES

PROCEDURE FOR LINE CLEARANCES OBJECTIVE: To ensure that the area, equipment and activities required for the manufacturing and packing of pharmaceutical products are free from any potential sources of cross contamination / mix-ups (Line clearance). 2.0 SCOPE: The line clearance procedure is applicable to all the activities including dispensing, manufacturing, packaging and related activities. 3.0 Responsibility … Read more