Learn about Installation Qualification, Operational Qualification and Performance Qualification (IQ OQ PQ) in the Pharmaceutical industry. Introduction (IQ OQ PQ) In the pharmaceutical sector IQ OQÂ PQ are utilized throughout validation procedures.Installation qualification, operational qualification, […]
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Learn how to write a SOP for Internal Audit and self inspection in the pharmaceutical industry. 1. PURPOSE To describe a standard procedure to give a planned and systematic examination and check of a system,
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“Explore the intricacies of Supply Chain Management (SCM) in the pharmaceutical industry, from sourcing raw materials to delivering life-saving medications. Dive into challenges, innovations, and the critical role of logistics in ensuring patient safety and
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Pharmaceutical Microbiology plays a significant role in the pharmaceutical industry, ensuring the safety and quality of pharmaceutical products. Introduction Microbiology has an applied subfield that includes pharmaceutical microbiology. It involves the study of microorganisms involved
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Precision medicine, also known as personalized medicine, is an innovative approach to medical treatment and healthcare that takes into account individual differences in patients’ genes, environments, and lifestyles. The goal of precision medicine is to
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The product management department serves as the driving force behind the development, launch, and ongoing management of pharmaceutical products. Introduction Product management plays a crucial role in the pharmaceutical industry as it drives innovation, ensures
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Know here about validation protocol writing techniques in pharmaceuticals. When writing a validation protocol in the pharmaceutical industry, it’s important to follow certain guidelines and include specific elements. Here’s a step-by-step guide on how to
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Learn how to write a standard procedure for Concurrent Process Validation in the Pharmaceutical Industry. 1.0 PURPOSE To describe standard procedure for Concurrent Process Validation of all products in the pharmaceutical industry. 2.0 SCOPE This
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I wanted to discuss the importance of Annual Product Quality Review (APQR) in the pharmaceutical industry. APQR is a crucial process that ensures the continuous evaluation and improvement of pharmaceutical product quality, safety, and efficacy.
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Learn how to prepare a standard procedure for Annual Product Quality Review (APQR) in Pharmaceuticals. 1.0 PURPOSE To describe a standard procedure that gives guidance for Annual Product Quality Reviews (APQRs) of all pharmaceutical products
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Learn how to prepare a procedure for Qualification of Autoclave in the microbiology Laboratory. 1.0 PURPOSE To describe the procedure for qualification of autoclave machine in a microbiological laboratory. 2.0 SCOPE This SOP is applicable
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The decision to compile all Quality, Safety, and Efficacy data into a single document, known as the CTD (Common Technical Document), standardized electronic filing transformed the regulatory review processes and made it possible to follow
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Optimize inventory control with FIFO, LIFO, FEFO Methods. Prioritize profitability and product quality. Learn their benefits and choose the right strategy. Introduction To establish the sequence in which products are sold or used, FIFO, FEFO,
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Learn how to write and prepare SOP for Preventive Maintenance of DM (Demineralized) Water Plant in the pharmaceutical industry. 1.0 PURPOSE To give instructions on how to make procedures for preventive maintenance of DM plant.
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PPIC stands for “Production Planning and Inventory Control” in the context of the pharmaceutical industry. It refers to the systematic process of managing and optimizing production activities and inventory levels within a pharmaceutical manufacturing or
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Study the significance of GxP in the pharmaceutical industry. Learn about GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and other standards. Ensure product quality and compliance. What is GxP in pharma? GxP refers to a series of
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Learn how to write SOP for Growth Promotion Test (GPT) of Culture Media to streamline laboratory procedures. Assure accurate and trustworthy media quality evaluation outcomes. 1.0 PURPOSE To describe the Standard Operating Procedure for Growth
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Learn how to write an SOP for Maintenance of Stock Cultures in the Microbiology Laboratory of Pharmaceuticals. 1.0 PURPOSE To describe the procedure for maintaining stock cultures in a microbiological laboratory. 2.0 SCOPE This SOP
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Learn how to write SOP for Receiving of Raw and Packaging Materials in the warehouse. 1.0 PURPOSE To set up the procedure for receiving and inspecting incoming raw and primary packaging materials in the warehouse.
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Learn how to prepare a SOP for Labeling of Raw and Packaging Materials in pharmaceuticals. 1.0 PURPOSE To set up the procedure for labeling & affixing labels to raw materials in the warehouse. 2.0 SCOPE
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