The Pharmaceutical Marketing System involves many strategies used to promote pharmaceutical products, including direct sales, digital marketing, and healthcare professional outreach. With a focus on global share, it examines the market distribution, competition, and trends […]
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Learn how to write a standard procedure SOP for calibration of UV-Vis Spectrophotometer in quality control laboratory. 1. PURPOSE To outlines the steps for the calibration of the UV-Vis Spectrophotometer to ensure accurate and precise
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Learn how to write a standard procedure SOP for calibration of FTIR apparatus (Fourier Transform Infrared) Spectrometer in quality control laboratory. 1. PURPOSE To describes the steps for the proper calibration of the Fourier Transform
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Learn how to write a standard procedure SOP for calibration of HPLC (High-Performance Liquid Chromatograph) in quality control laboratory. 1. PURPOSE To describes the procedure for the calibration of the High-Performance Liquid Chromatograph (HPLC) used
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Learn how to write a standard procedure SOP for calibration of dissolution test apparatus in quality control laboratory in pharmaceuticals. 1. PURPOSE To describe of this Standard Operating Procedure (SOP) is to provide a standardized
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MACO (Maximum Allowable Carryover) Calculation is a key function in cleaning validation to determine the acceptable level of residue of a previous product that can be carried over to the next product without risking patient
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HPLC column cleaning solutions used in High-Performance Liquid Chromatography (HPLC) columns depends on the type of contaminant and the column material (silica-based, C18, or other specialized phases). Below are the general guidelines for cleaning solutions
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Learn how to write a standard cleaning validation report of microbiology laboratory in pharmaceuticals. 1. Objective The purpose of this validation report is to evaluate and confirm the effectiveness of cleaning procedures applied in the
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Learn about the cleaning validation protocol for microbiology lab of cleaning validation process in the pharmaceutical industry. 1. Objective The purpose of this Cleaning Validation Protocol is to define the procedures for verifying that cleaning
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Learn about Propylene Glycol vs Ethylene Glycol means the key differences between propylene glycol and ethylene glycol, including their chemical properties, uses, toxicity levels, and safety. Discover which is safer for various applications and industries.
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Propylene glycol (PG) is a synthetic organic compound widely used in the pharmaceutical industry. It plays a significant role in various formulations due to its versatile properties, contributing to the effectiveness, stability, and safety of
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Learn about the cleaning validation protocol for quality control laboratory area of cleaning validation process in the pharmaceutical industry. 1. Introduction Cleaning validation is a critical part of quality assurance in pharmaceutical manufacturing. The purpose
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Learn about the cleaning validation protocol for production area of cleaning validation process in the pharmaceutical industry. 1. Introduction This protocol defines the procedures for cleaning validation of the production area in accordance with Good
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A Cleaning Validation Master Plan (CVMP) outlines the strategy, processes, and protocols to ensure equipment cleaning meets regulatory standards in pharmaceutical manufacturing, preventing contamination and ensuring product safety. 1. Introduction The Cleaning Validation Master Plan
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Learn the role of pharmacists in patient management as outlined by the World Health Organization (WHO). Who is pharmacist? A pharmacist is a healthcare professional responsible for preparing, dispensing, and advising on medications, ensuring their
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Learn how to write a standard operating procedure SOP for vendor audit (supplier audit) to select vendor or supplier in pharmaceutical. 1.0 PURPOSE To evaluate a potential new source or to monitor ongoing quality on
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Explore the principles & applications of Fluid Bed Dryer(FBD), a crucial technology in the pharmaceutical industry. Learn about the principles, mechanism, benefits, and key applications of FBDs for efficient drying and processing of powders, granules,
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Learn how to handle audits in pharmaceutical industry. Handling audits, whether internal or external (by regulatory authorities or clients), requires careful planning, preparation, and a systematic approach. Here’s a step-by-step guide to successfully handle audits:
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Learn how to prepare and standardize 0.5 N Hydrochloric acid VS (Volumetric Solution) as per the United States Pharmacopoeia (USP) in the quality control laboratory. Materials Required 1. Hydrochloric acid (HCl) 2. Carbon dioxide-free water
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Learn how to prepare and standardize 0.1 N Hydrochloric acid VS (Volumetric Solution) as per the United States Pharmacopoeia (USP) in the quality control laboratory. Materials Required 1. Hydrochloric acid (HCl) 2. Carbon dioxide-free water
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