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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Learn how to write standard procedure for sampling method of packaging materials in the pharmaceutical industry. 1. PURPOSE The purpose of this procedure is to describe sampling method of packaging materials for ensuring the identity
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There are difference between drugs and medicines difference. However, we often convey the same concept with these phrases. But, there are a few distinctions between a drug and a medicine, and these include: 1. Definition
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Learn how to write a standard SOP for chemical laboratory safety in the pharmaceutical industry. 1. PURPOS To describe the safety procedures in the chemical Laboratory. 2. SCOPE This procedure applies for handling of all
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Learn how to write a standard batch numbering SOP for finished products in the pharmaceutical industry. 1. PURPOSE To describe a batch numbering system and how to assign a unique batch number for eachpharmaceutical finished
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Calibration in the pharmaceutical industry is an important process. It refers to ensure the accuracy and precision of instruments and equipment used in manufacturing, testing, and quality control. Proper calibration ensures that the data generated
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This is a comprehensive overview of common tablet defects as well as information on effective remedies. Tablet quality and efficacy are essential factors in pharmaceutical manufacturing. For high standards to be confirmed, it is important
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A Stability Study Protocol outlines procedures to assess a product’s shelf life under various conditions, ensuring its quality, safety, and efficacy over time through systematic testing and analysis. 1. DEFINITION This proposal was developed within
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Learn how to write a standard specification and Test Procedure for analysis of Azithromycin Tablet 500 mg. STANDARD SPECIFICATIONS FOR GRANULES This specification is checked at the end of the granulation stage. Sl. No. Tests
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Learn how to write a SOP for sampling method of raw materials in sampling booth. 1. PURPOSE The purpose of this procedure is to describe sampling method of raw materials for ensuring the identity and
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Learn how to write a standard cleaning procedure of production area in pharmaceutical industry. 1. PURPOSE To describe a proper house-keeping & cleanliness at the production areas for minimizing contamination 2. SCOPE This procedure is
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Learn how to write a standard procedure for Cleaning of QC laboratory (Quality Control laboratory) in pharmaceuticals. 1. PURPOSE The purpose of this procedure is to describe frequency and procedure for cleaning Quality Control Laboratory.
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