Learn how to prepare and standardize 0.5 N Sodium Hydroxide VS (Volumetric Solution) as per the United States Pharmacopoeia (USP) in the quality control laboratory. Materials Required 1. Sodium hydroxide (NaOH) pellets (high purity) 2. […]
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In pharmaceutical industry tablet manufacturing process is a complex method that involves several stages blending, granulation, compression, Coating and packaging to ensure that the final product is of high quality, meets regulatory standards, and is
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The theme for World Pharmacists Day 2024, celebrated on September 25, 2024, is “Pharmacists: Meeting Global Health Needs”. This theme, announced by the International Pharmaceutical Federation (FIP), highlights the vital role pharmacists play as integral members
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The pharmaceutical industry continues to be a major driver of healthcare innovation, with the top companies generating significant revenue through the development of new treatments and medicines. Here’s a detailed look at the global top
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Discover the total registered list of pharmaceutical company in Bangladesh up to 2024. The pharmaceutical industry in Bangladesh is one of the most rapidly growing sectors, playing a vital role in the country’s economic development
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Learn about the detailed manufacturing process of Benzoic Acid and Salicylic Acid ointment, including formulation steps, ingredients and preparation techniques to ensure effective treatment of skin infections and fungal conditions. It is the most popular
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In pharmaceutical manufacturing, reviewing BMR (Batch Manufacturing Records), BCR (Batch Coating Records) , and BPR (Batch Packaging Records) is essential to ensure compliance with Good Manufacturing Practices (GMP), ensure product quality, and maintain regulatory standards.
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Know the benefits of zinc shampoo for relieving an itchy scalp and reducing hair loss. Learn how zinc’s antifungal and soothing properties can promote a healthier scalp, reduce dandruff, and strengthen hair follicles for improved
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In the pharmaceutical sector, validation is an essential part of quality assurance. It entails a methodical process of creating written proof that a certain method, tool, system, or equipment reliably yields outcomes that adhere to
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To register a new pharmaceutical company and obtain the necessary licenses, you typically need to follow a series of steps that ensure compliance with local, regional, and international regulations. The general steps in the registration
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Computer-Aided Drug Design (CADD) is a field that leverages computational methods to discover, develop, and analyze drugs and active molecules. CADD can significantly reduce the time and cost associated with drug discovery and development by
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This SOP ensures that the formulation development process is conducted systematically and consistently, following best practices and regulatory requirements to ensure the quality and safety of the final drug product. 1. PURPOSE To describe the
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Learn how to write a standard procedure for stability testing in pharmaceuticals, including guidelines for sample preparation, storage conditions, and data analysis to ensure product quality and safety. 1. PURPOSE To describe the procedures for
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Learn the key difference between water and moisture content, including their definitions, measurement methods, and applications in pharmaceuticals industry. Understand how these terms impact material properties and quality control. 1. Water Content Definition: Water content
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Learn how to write a standard procedure for Product Development Planning in pharmaceutical industry. 1. PURPOSE To outlines the steps and guidelines for planning product development, ensuring that all necessary tasks are completed in a
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A Validation Report is a comprehensive document that summarizes the results of validation activities, confirming that a process, system, or equipment consistently performs according to predefined specifications. It serves as evidence of compliance with regulatory
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CAPA stands for Corrective Action and Preventive Action. It is a systematic process used in the pharmaceutical industry to identify, correct, and prevent issues that can affect product quality, safety, or regulatory compliance. Corrective Action
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A Validation Schedule is a documented plan that outlines all the validation activities a pharmaceutical manufacturing facility must perform over a specific period. It ensures that all critical processes, equipment, systems, and procedures are consistently
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Learn how to prepare Cefixime Trihydrate PFS formulation and manufacturing process that ensures high-quality and reliable production in the pharmaceutical industry. Product Name: Cefixime Trihydrate PFS 50 ml bottle Concentration: Cefixime Trihydrate USP 200 mg
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Learn how to prepare Azithromycin PFS formulation and manufacturing process that ensures high-quality and reliable production in the pharmaceutical industry. Product Name: Azithromycin PFS Concentration: Azithromycin USP 200 mg / 5 ml Batch Size (Kg):
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