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Sunday, August 24, 2008

Who guide lines for Pharmaceutical manufactureres

I hope you all are liking my posts on Who Guideline for Pharmaceuticals Manufacturers ,rather for a WHO GMP pharamceutical manufacturing plant.
I have posted my earlier posts about.
1.Cleaning validation and its Sop. i have given in details required for validation for cleaning.
2.I have writen about Water System Validation , i have given a sample of water system validation report and protocol.
3.I have posted about Air Handling Systems .and also some who guide lines on injectables .
Just chill your self and and brows through my posts you will find almost every thing you want .More over you can ask me for a specific topic , i will like to prvide you the details here.
My intrest of topic is pharmaceuticals ,and research , i am also writing on HIV , AIDS ,research , if any new thing developed , you will see this on website

In coming posts i am going to write about
Master Manufacturing Document .
Master Formula Card.
Master Formula Record.
If you have any thing to shair , please do write me on, i will be happy to post it.
Following are some of articles which;will be useful for you in further understanding of aspects of sterile dosage form manufacturing

Pharmaceutical Validation

Cleen Room Classification

Pharmaceutical Industry

Pharmaceutical Manufacturing

Clinical Trials

To Find Pharmaceutical jobs and make a Pharmaceutical careers see here pharmaceutical companies

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