Ankur Choudhary

Ankur Choudhary

Ankur Choudhary is an experienced pharmaceutical blogger and founder of Pharmaceutical Guidelines.

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Ankur Choudhary Free Articles

Annual Product Review in Pharmaceuticals

Annual product quality review is an quality tool used to determine the quality of the product for a period of one year. It gives an overall idea for the quality of the manufactured product.

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Line Clearance in Pharmaceuticals

Line clearance is an important system in pharmaceutical manufacturing. It ensures the process as per the standard operating procedure. Quality assurance is responsible for the line clearance in manufacturing area.

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Terminal Sterilization Process

Terminal sterilization is a process whiched is followed after the end of the manufacturing of the sterile pharmaceutical products. This process helps to assure the sterility of the finished goods.

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Steps to Write Standard Operation Procedures

Standard operating procedure is an written document to carry out any process in the company. It has all the ingormation regarding the process including the operating procedures of the instrument and equipment.

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Determination of Biological Oxygen Demand (BOD)

Biological oxygen demand is used to determine the biological load in the waste water. Higher BOD indicates the high microbial load in water.

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Reverse Osmosis Process for Water Purification

Reverse osmosis process is widely used for water purification. RO membranes are very fine and have very small pore size.

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Sterility Assurance Level and D value

Sterility assurance level is the assurance of the sterility of the sterilized materials. It provides the data to believe that the sterilization is done properly.

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Validation Master Plan in Pharmaceuticals

Validation Master Plan (VMP) is an internal planing of the departments for the validation of instruments used in that department. It cintains all informations about the validation process of the instrument and equipments in the department.

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Vendor Qualification Procedure for Pharmaceutical

Vendor qualification is an important factor for the regulatory point of view. All raw materials and packing materials vendors must be qualified as per the appropriate procedure.

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Current Good Manufacturing Practices in Pharmaceutical Manufacturing

Good manufacturing practices (GMP) is an working style in pharmaceutical manufacturing that helps to maintain the quality of the pharmaceutical products.

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Validation in Pharmaceutical Manufacturing

Validation of pharmaceutical process and methods is a mandatory requirement for regulatory audit compliance. All methods and methods are validated for their cinsistancy.

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Cleanrooms and Air Changes in Pharmaceuticals

Cleanrooms are the areas for sterile products manufacturing. These area have less contamination in than the open area and air changes are the number of changes in the whole air of the sterile area.

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Preparation of Buffer Solutions in Pharmaceuticals

Buffers are solutions having the stable pH value. these are used for the pH stability of the solution where the pH of the solution changes as tme passes.

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Analytical Method Validation (AMV) in Pharmaceuticals

All analytical methods implimented for the analysis of the pharmaceutical drugs should be validated properly. It will help to obtain the accurate results.

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Humidity and Working of Hygrometer

Temperature and humidity in pharmaceutical manufacturing are important parameters that can influence the product quality. Hygrometer is a useful device to measure the relative humidity in manufacturing cubicle .

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