Monday, April 13, 2009

Water system validation Purified water system validation document

Water system validation sample document Purified water system DQ IQ PQ and actual validation document sample Guide for Quality assurance in Pharmaceuticals

Dear friends today we will like to share with you a very important document in pharmaceuticals manufacturing , water system validation.
Water is very important constituent of any pharmaceutical and its systems are maintained with very much care in our pharmaceuticals manufacturing units.
So i am giving a sample document for purified water system in pharmaceuticals manufacturing company.
There is given Complete protocol for water system validation and concurrent validation report for water system, protocol for chemical as well as microbiological validation of purified water system, it consist of only Anion bed, cation bed and mixed bed ion exchange resign columns for purification of water , in sample document reverse osmosis column is not available , data is similar , you should insert additional data rows and columns there , though this is very little it will definitely provide you some help or provide you some knowledge over this topic.

This contains a spread sheet which you can copy and paste in a new spreed sheet and use it for your self as a reference or make changes in that and use it for your self.
So here is this document

Water system validation , Purified Water System Validation

We have written a very informative article about Reverse Osmosis (RO) Water system in Pharmaceuticals

Also you we have published article about how to prepare water for injection , sterile water for injection 

Also here is very important information given over here about
Checke list for inspection and Quality audit of your pharmaceutical manufacturing unit
Copy and paste in fresh spread sheet with keep destination formatting.
Also refer on this blog , you will find lot of very useful sources for your knowledge and i have given lot of information about
Quality assurance in pharmaceuticals
GMP , c GMP , sterile dosage form manufacturing , injectables,
Questions and answers for training of your staff and workers ,
Air handling systems in pharmaceuticals ,
clean room requirements , clean rooms ,
Real time stability studies , Accelerated stability studies ,
Sterility testing , toxicity testing ,
WHO guidelines , Cleaning validation,
Pharmaceutical product validation ,Master manufacturing Documents,
Dosser for Pharmaceutical Product registration ,Quality assurance systems .
So find all these here .

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Posted by: Martin

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