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
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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,
Calibration in the Pharmaceutical Industry Read More »
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
Common Tablet Defects and Remedies in Manufacturing Read More »
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
Stability Study Protocol Template of Tablet Read More »
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
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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
SOP For Sampling Method of Raw Materials Read More »
Learn how to write a standard cleaning procedure of production area in pharmaceutical industry. 1. PURPOSE Â To describe a proper house-keeping & cleanliness at the
SOP For Cleaning Procedure of Production Area Read More »
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
SOP for Cleaning of QC Laboratory Read More »
Learn how to write a procedure for cleaning of sampling tools used for sampling in pharmaceuticals. 1. PURPOSE The purpose of this procedure is to
SOP for Cleaning of Sampling Tools Read More »
Beta-lactam test for sensitivity of antibiotics, such as penicillin and cephalosporin in pharmaceutical, is vital for personnel working in environments where these antibiotics are frequently
Beta-lactam Test for Personnel in Manufacturing Read More »
After production, cloudiness problem in DNS IV infusion (Intravenous Dextrose Normal Saline) may be a sign of contamination, instability, or other problems that could hazard
DNS IV Infusion Post-Manufacturing Cloudiness Problem Read More »
Learn how to write a (Standard Operating procedure) SOP for training records of employees in the pharmaceuticals. 1. PURPOSE To describe a standard procedure of
SOP for Training Records Read More »
Learn how to write a (Standard Operating procedure) SOP for training and evaluation of the employees in the pharmaceuticals. 1. PURPOSE To describe the standard
SOP for Training and Evaluation of the Employee Read More »
Learn about Installation Qualification, Operational Qualification and Performance Qualification (IQ OQ PQ) in the Pharmaceutical industry. Introduction (IQ OQ PQ) In the pharmaceutical sector IQ
IQ OQ PQ in the Pharmaceuticals Read More »
Learn how to write a SOP for Internal Audit and self inspection in the pharmaceutical industry. 1. PURPOSE To describe a standard procedure to give
SOP for Internal Audit Read More »