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Monday, February 18, 2019
 
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Ankur Choudhary

Premium Author Ankur Choudhary

India

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


ARTICLES BY ANKUR CHOUDHARY


Titration is a basic analytical method to determine the potency of any material. It is widely used in pharmaceutical and chemical industries.
A good CV can help to find a good job. Your CV should contain all important parts including qualification, professional skills and achievements.
All doucments should be maintained properly as per the standard operating procedure. It should be applied for both printed and electronic documents.
Lubricants used for lubrication of pharmaceutical equipments must be of food grade. Other than food grade lubricants can be harmaful for the human health.
FDA forms are used to communicate the observation during the FDA inspections. Different forms are used as per the audit requirements.
Media fill validation is used to prove the strility of the manufacturing process in sterile pharmaceuticals.
Buffer solutions are used in the analysis of the pharmaceutical products and ingreadients to stable the pH of the solution.
Pharmaceutical product analysis is done by HPLC but before starting the analysis analytical method is developed. These methods should be validated before use.
Standard operating procedures have all informations about the process and the instruction to operate the instruments. These are written by the concerned department of pharmaceutical manufacturing unit...
Process validation is an important part of the pharmaceutical manufacturing process. All manufacturing processes are validated before there implementation.
Aresenic is analysed in all pharmaceuticalpreparations because arsenic is harmful for health and it can cause verious diseases.
Growth promotion test is helpful to prove that culture media is supporting the microbial growth. It is important to check every media or growth promotion test before its use.
All pharmaceutical cleaning procedures of pharmaceutical equiments should be validated. These cleaning methods should be validated before its application in manufacturing process.
Sterile area in pharmaceuticals is also known as creanroom area. this area should be qualified and validated before starting its use.
It is complicated to maintain the cleanroom areas because it is critical to maintain the areas. All cleanroom areas should be maintained properly to produce the best pharmaceutical products.








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