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USFDA WHO GMP Guidelines Pharmaceutical Regulations Information about Pharma Quality Managment System Validations Process Validation Cleaning Validation Equipment Qualification Equipment Process Validation Computer System Validation Sterile Product Manufacturing Guidelines Media fill guideline Aseptic Techniques in Sterile dosage form Clean Room Clean Room Classification Guidelines on Area Qualification HVAC AHU HEPA Filter HEPA Filter integrity testing and leak test

Friday, April 10, 2009

pharmaceuticals purified water system validation

This website is a guide for pharmaceuticals manufacturing we are happy to provide sample documents on following topics



Validation of Cleaning process Master document sample


pharmaceuticals water system validation sample document

Water system validation sample document Purified water system DQ IQ PQ and actual validation document sample (Copy and paste in excel , in pasting option select match destination formatting)



Change control In pharmaceuticals master document as a sample



SOP for Microbiology (Copy and paste in excel , in pasting option select match destination formatting)



Sample Document of Installation Qualification of a pharmaceutical machinery



Pharmaceutical Product validation master plan.

Checke list for inspection and Quality audit of your pharmaceutical manufacturing unit

You will find in latest post over this website about
Aseptic processing of sterile dosage forms and injections
Containers and closures for injection
Stability testing and finding expiry date of a pharmaceutical product by accelerated stability studies.
Sterility testing for Injectable dosage form (SEARCH IN BLOG ARCHIVE ON THIS WEBSITE)
What is pyrogen Detail information about pyrogen testing Toxicity studies
Detail information is provided on following topics
WHO GMP guidelines for pharmaceuticals with respect to premises , personnel, hygiene, and training , machinery , Quality control and Quality assurance , Air handling system ,clean rooms in critical aria and its particle control in air, prevention of cross contamination .etc
WHAT YOU NEED TO DO IS SEARCH OVER BLOG ARCHIVE YOU WILL FIND EVERY THING ON PHARMACEUTICALS HERE .
Its our privilege to serve every one associated with pharmaceutical manufacturing through this medium on pharmaceuticals guidelines for GMP and Quality assurance in pharmaceuticals.

we will like to keep today's post as a short but great informative for pharmaceutical manufacturers and pharma manufacturing pharmacists around the world , our authors intentions are to shair and provide knowledge on pharmaceuticals manufacturing processes , and its Quality assurance for producing best quality pharmaceuticals to serve human beings.

we have given few links above and below to some very important topics in pharmaceuticals manufacturing and its documentation as a sample reference documents .

These documents you can simply copy in to word file and use it for your self do some up gradation too .

We have given these documents earlier on this website but again we are giving them here as this website is very big in its content on pharmaceuticals , all most all topics in pharmaceuticals manufacturing is written over here ,

What you have to do is search on blog archive for who gmp guidelines , quality assurance guidelines , but some important documents are here as sample documents



Validation of Cleaning process Master document sample

pharmaceuticals water system validation sample document

Water system validation sample document Purified water system DQ IQ PQ and actual validation document sample (Copy and paste in excel , in pasting option select match destination formatting)

Change control In pharmaceuticals master document as a sample

SOP for Microbiology (There are two sheets there copy and paste in excel , in pasting option select match destination formatting)

Sample Document of Installation Qualification of a pharmaceutical machinery

Pharmaceutical Product validation master plan.

Checke list for inspection and Quality audit of your pharmaceutical manufacturing unit

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This website consist of detail Information about Pharma Guidelines Pharma Regulatory Affairs USFDA Guidelines WHO Guidelines Pharmaceutical Quality Management System Pharma Validations Process Validation Cleaning Validation Equipment Qualification Equipment Process Validation Computer System Validation Sterile Product Manufacturing Guidelines Media fill guideline Aseptic Techniques in Sterile dosage form Clean Room Clean Room Classification Guidelines on Area Qualification HVAC AHU HEPA Filter HEPA Filter integrity testing and leak test