Tag Archives: West Dunbartonshire

Facility Validation in pharmaceutical Pharma Company

Facility Validation in pharmaceutical Pharma Company Facility qualification (a part of validation that proves and documents that equipment or ancillary systems are properly installed, work correctly, and actually lead to the expected results), and validation (establishing documented evidence that provides a high degree of assurance that the manufacturing processes, including …

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How to face Interview

How to face Interview Remember, you never get a second chance to make a good first impression. However, good preparation takes the pain out of the process. Interview Preparation Remember: Prepare, prepare, prepare! Preparation is essential and greatly enhances your chances of performing well, So: know your CV know your …

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SOP for Operational qualification protocol of Blister Packing Machine (BQS)

SOP for Operational qualification protocol of Blister Packing Machine (BQS) PURPOSE To describe the Operational Qualification procedure to be used during qualification of Blister Packing Machine (BQS), its accessories and to define the specification of the sytem in order to: Ensure that the equipment meets the Operational/Design limits as per …

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SOP For Design Qualification of Colloid Mill

SOP For Design Qualification of Colloid Mill OBJECTIVE To design, engineer, and supply the Colloid Mill and to provide assurance that the machine is manufactured and it comply with the Scope of Supply. To prove that each operation proceeds as per the design qualification and the tolerances prescribed there in …

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SOP For Installation qualification of 300 L Gelatin Melting Reactor

SOP For Installation qualification of 300 L Gelatin Melting Reactor PURPOSE: To describe the Installation Qualification of 300 L Gelatin Melting Reactor its accessories and to define the Specification of the system in order to: Ensure that the equipment meets the specification as per Design Qualification. Aid verification of the …

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SOP for Design Qualification of Blister Packing Machine (Model – BQS)

SOP for Design Qualification of Blister Packing Machine (Model – BQS) OBJECTIVE To design, engineer, and supply the Blister Packing Machine  (Model: BQS) and to ensure that it complies with the Scope of Supply. To prove that each operation proceeds as per the design specification and the tolerances prescribed there …

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SOP for Sampling of In-process blends, uncoated tablets, coated tablets and filled capsules

SOP for Sampling of In-process blends, uncoated tablets, coated tablets and filled capsules OBJECTIVE : To provide a procedure for representative sampling of  In-process blends, uncoated tablets, coated tablets and filled capsules. RESPONSIBILITY : Officer – Quality Assurance. Head – Quality Assurance to ensure compliance. PROCEDURE : After receiving the …

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Installation qualification of Blister Packing Machine (Hoonga)

Installation qualification of Blister Packing Machine (Hoonga) PURPOSE To describe the Installation Qualification procedure to be used during qualification of Blister Packing Machine (Hoonga), its accessories and to define the Specification of the system in order to Ensure that the equipment meets the specification as Design Qualification. Aid verification of …

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SOP for Operational qualification protocol of Gelatin Melting Reactor

SOP for Operational qualification protocol of Gelatin Melting Reactor PURPOSE: To describe the Operational Qualification of 300 L Gelatin Melting Reactor, its accessories and to define the specification of the system in order to: ensure that the equipment meets the Operational/Design limits as per user requirements. ensure that the equipment …

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SOP for Operational Qualification of Capsule Printing Machine

SOP for Operational Qualification of Capsule Printing Machine PURPOSE:  To describe the Operational Qualification of Capsule Printing Machine its accessories and to define the specification of the system in order to: ensure that the machine meets the Operational / Design limits as per user requirements ensure that the machine will …

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SOP for Design Qualification of Capsule Printing machine

SOP for Design Qualification of Capsule Printing machine OBJECTIVE To design, engineer, and supply the Capsule Printing Machine and to provide assurance that the machine is manufactured as per the URS and it comply with the Scope of Supply. To prove that each operation proceeds as per the design qualification …

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SOP for Installation Qualification of Capsule Printing machine

SOP for Installation Qualification of Capsule Printing machine PURPOSE To describe the Installation Qualification of Capsule printing machine, its accessories and to define the Specification of the system in order to: Ensure that the equipment meets the specification as per Design Qualification. Aid verification of the installation as per equipment …

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SOP FOR OPERATIONAL QUALIFICATION of Soft Gelatin Encapsulation System

SOP FOR OPERATIONAL QUALIFICATION of Soft Gelatin Encapsulation System PURPOSE To describe the Operational Qualification of Arbes Encapsulation System (CAP-X-8) along with Tumble Dryer and Gravity Feed Pipes, its accessories and to define the specification of the system in order to: ensure that the equipment meets the Operational/Design limits as …

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SOP on Training

SOP on Training Objective:  To lay down a procedure to conduct training of working personnel at all levels and its evaluation. Scope:  This Standard Operating Procedure is applicable for the training personnel at Pharmaceuticals Companies. Responsibility Head, QA, or his/her designee for coordination on the training of the personnel. The …

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SOP on Drug Product Recalls

SOP on Drug Product Recalls OBJECTIVE : To define the procedures used to effect the recall of a marketed product once it has been decided that such a course of action is required. RESPONSIBILITY : The  Managing  Director and  Divisional  Head shall be responsible for making the decision that a  …

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Issuance and Evaluation of Product Exception Investigation Reports (“EIRs”).

Issuance and Evaluation of Investigation Reports OBJECTIVE : To establish a documentation system by which qualified representatives report  and investigate the exceptions of drug products in the manufacturing process, in-process specifications. RESPONSIBILITY : Executive – Production/Packaging to prepare the Exception Investigation Report (EIR). Head – Production to investigate and implement …

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SOP on Process Validation Programmed in Pharmaceutical Company

SOP on Process Validation Programmed in Pharmaceutical Company OBJECTIVE : To lay down the procedure for the process validation of products to ensure that a specific process will consistently produce the product meeting its pre-determined specifications and quality attributes. RESPONSIBILITY : Research  Development to prepare and execute the validation protocol …

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Preparation, Approval, Issue and Control of Art works for labeling of Pharmaceutical products

Preparation, Approval, Issue, and Control of Artworks for labeling of Pharmaceutical products OBJECTIVE : To lay down the Procedure for Preparation, Approval, Issue, and Control of artworks for labeling of pharmaceutical products. RESPONSIBILITY : R&D(Packaging Development) to prepare the Artwork, positive or soft copy, and procure shade cards & specimens …

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Calibration for Weighing Balances

Calibration for Weighing Balances In various industries, such as pharmaceuticals, laboratories, manufacturing, and research, precise measurements are of utmost importance. Weighing balances are essential instruments that enable us to obtain accurate measurements, making them crucial in ensuring the quality of products, integrity of research, and compliance with regulatory standards. Calibration …

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Calibration procedure for halogen moisture analyzer

Calibration procedure for halogen moisture analyzer OBJECTIVE To lay down the procedure for calibration of the Halogen moisture analyzer, SCOPE This SOP shall provide the calibration procedure of the Halogen moisture analyzer in the in-process quality assurance department and quality control department. RESPONSIBILITY Officer/ Executive – Quality Control/Quality Assurance. ACCOUNTABILITY …

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