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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Learn how to prepare a SOP for Dress Changing Procedure of Personnel in Warehouse of Pharmaceutical. 1.0 PURPOSE To describe the entry and exit procedures in the warehouse. 2.0 SCOPE This SOP applies to people
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Learn How to Write SOP for leak test of HEPA filters in Pharmaceutical plants. 1.0 PURPOSE To give instructions on how to make sure HEPA filters are functional and intact. 2.0 SCOPE This SOP is
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Learn how to write an SOP for the Planned Preventive Maintenance schedule of process and utility equipment in the pharmaceutical plant. 1.0 PURPOSE The purpose of ‘Preventive Maintenance’ is to carry out maintenance on equipment
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