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The SOP for the operation of the Effluent Treatment Plant (ETP) and Sewage Treatment Plant (STP) to define the comprehensive procedure for handling the waste of pharmaceuticals. Effluent Treatment Plant (ETP) – The mechanism or process used to treat the wastewater prior to release into the environment or its reuse. Sewage Treatment Plant (STP) -It […]

Annual Product Review (APR) is the requirement of various regulatory agencies. APR roots the monitoring of product quality as well as finding out the scope of quality improvement by controlling the critical process parameters (CPP). Visit to copy this SOP APR – Annual Product Review also known as APQR – Annual Product Quality Review and […]

LAF : Laminar Air Flow –  Airflow which is linear and positive up to working surfaces and thus prevents contamination of surrounding viable/ non viable particulate matter in aseptic handling. The Operation, Cleaning, Maintenance and Qualification of Laminar Air Flow (LAF) shall discussed in below SOP. Laminar Air flow (LAF) – Operation, Cleaning and Qualification […]

Calibration of UV spectrophotometer (UV-VIS Spectrophotometer) for all parameters as per IP, BP and USP pharmacopoeia like, Internal Calibration, Match pairing of UV cell / cuvette, Control of wavelength, control of Absorbance, Limit of Stray light, Resolution and Resolution Power, Linearity Study and 2nd derivatives. UV Calibration / Calibration of UV Spectrophotometer : Parameters : […]

Cleaning and sanitization of Utility system and Equipment is crucial to maintain the Quality of the drug product and to avoid the cross contamination also Standard Operating Procedure for Cleaning and Sanitization PURPOSE: The purpose of this Standard Operation Procedure is Defines the requirements Ensure that facility and Equipment Cleaning and Sanitization are managed and […]

In Pharmaceutical industries Quality Control (QC) is believe as one of the most vital department.It acts as a barrier between the manufacturing unit and Market to ensure the Quality of the manufactured product. In Quality Control Functions Large numbers of employees are work together in QC department at different grade with a common Aim, which […]

The Quality Control Laboratory in the Pharmaceutical plants plays the critical role to maintain, monitor and consistent product of Pharmaceutical products. In the laboratory from starting material to finished products being tested at the different manufacturing stages. Good Laboratory Practices assist to perform the timely and accurate analytical results. In the day to day activities […]

Quality Assurance Department Functions in Pharmaceuticals : Quality Assurance Department shall function for assuring the quality of all the Products manufactured, at every stage of manufacturing / processing of Drug Products. This shall be achieved by performing the functions of monitoring as per the laid systems for the following areas which is not limited to […]

Cleaning of laboratory glassware is the key for success of an analysis in the Pharmaceutical Quality Control Laboratory. Even the maximum cautiously performed laboratory analysis can produced erroneous/wrong results if uncleaned glassware is being used during the analysis. If the glassware that is used for measuring solvent / sample solution or standard solutions is contaminated […]

This article is to describe the process and requirements regarding Sample Management in Quality Control Laboratory , including the receipt, handling, controls, maintenance, distribution for testing, and destruction. The implementation of this procedure provides documented records of the chain of custody for the test samples to ensure their accountability and tractability. This article (Laboratory Sample […]

A cleaning validation protocol shall be developed for the ‘worst case’ product selected for the cleaning validation program. Following information (but not limited to) the following included in the cleaning validation protocol. Numbering of the Cleaning Validation protocol shall be done through of respective SOP of Cleaning Validation Protocol Numbering. Cleaning Validation Protocol Format 1.0  […]

Introduction: The cleaning validation Master Plan will function as an umbrella guidance document for all the cleaning validation protocols, programs, and procedures adopted to ensure that all the equipment utilized for the manufacturing of tablets and hard gelatin capsules dosage form is cleaned up at an acceptable level. The Pharmaceuticals manufacturing entities engaged in the […]