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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Here are some interview questions and answers for PPIC (Production Planning & Inventory Control) in the pharmaceutical industry: Interview Questions and Answers for PPIC Describe PPIC in Pharmaceutical Industry. PPIC stands for “Production Planning and
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Learn how to write the Standard Operating Procedure (SOP) for basic GMP requirements in production area, ensuring quality and compliance in pharmaceutical manufacturing environments. 1. PURPOSE To describe a basic rules for Good Manufacturing Practices
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Learn how to write a standard SOP for disposal of rejected materials (raw and finished products) in the pharmaceutical industry. 1. PURPOSE The purpose of this procedure is to establish a system for the destruction
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Learn how to write a standard procedure for handling & usage of hazardous chemicals in quality control laboratory. 1. PURPOSE The purpose of this SOP is to describe the procedure handling & usage of hazardous
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