SOP for QMS Tools

SOP for QMS Tools Document Management –Review batch records, stability reports, validation reports, and associated documents required to comply with respective regulatory country GMP. Site Deviations – initiation, investigation, review, closeout, and maintenance for internal and external issues. Change Controls – initiation, review, closeout, and maintenance of all internal and external change controls. CAPA Management – manages … Read more

VALIDATION OF FREEZE DRYER

VALIDATION OF FREEZE DRYER “In freeze-drying, water is removed from the frozen state by sublimation, i.e., direct change of water from solid into vapor without conversion to a liquid phase”. Used for drying of a no. of products. Especially, Blood plasma and its fractionated products. Bacterial and viral cultures. Human tissues. Antibiotics and plant extracts. … Read more

Procedure For Annual Product Quality Review

Procedure For Annual Product Quality Review STANDARD OPERATING PROCEDURE Title : Procedure For Annual Product Quality Review OBJECTIVE    To lay down a procedure for Annual Product Quality Review. SCOPE This procedure is applicable to Quality Assurance Department for annual product review of finished products . RESPONSIBILITY Executive-Quality Assurance ACCOUNTABILITY Manager-Quality Assurance VP – Plant … Read more

Procedure For Product Recall

  Procedure For Product Recall STANDARD OPERATING PROCEDURE Title : Procedure For Product Recall          OBJECTIVE To lay down the Procedure for product recall. SCOPE This Procedure is applicable for Handling of Product Recalls at Pharmaceutical Company. RESPONSIBILITY It is a Joint responsibility of the Marketing Department in coordination with Quality Assurance Head-Export / Company Appointed Business agent of the country in coordination with Quality Assurance. Manager – Quality Assurance ACCOUNTABILITY Manager-QA VP-Plant & Operations. … Read more

Omeprazole 40 mg

Omeprazole 40 mg PURPOSE: This Standard Operating Procedure 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 SOP. The Production … Read more

Pantoprazole Sodium Sesquihydrate

Pantoprazole Sodium Sesquihydrate PURPOSE:  This Standard Operating Procedure 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 SOP. The … Read more

Norethisterone Tablet

Norethisterone 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 Production Pharmacist, … Read more

Metformin Hydrochloride Tablet 500 mg

Metformin Hydrochloride Tablet 500 mg: A Comprehensive Guide Metformin hydrochloride is a widely prescribed medication used to manage type 2 diabetes mellitus. It belongs to the class of drugs known as biguanides and is known for its effectiveness in controlling blood glucose levels. Metformin hydrochloride tablets in the 500 mg strength are commonly prescribed due … Read more

Clotrimazole Tablet

Clotrimazole 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 Production Pharmacist, … Read more

PARACETAMOL TABLET

PARACETAMOL 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 Production Pharmacist, … Read more