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Friday, July 25, 2008

Clean room in pharma industry.
Article is being revised to make it most updated and provide our readers complete detailed information about clean rooms

Clean Rooms and Air Handling Systems — Design for Compliance
with respect to WHO GUIDELINE , WHO GMP
clean rooms 
clean room
(HEPA)validation
ISO Class 5 room (Class 100 see Clean Room Classification)
 HEPA filters,
(also see Pharma Process Validation )
 money

FOR
WHO GUIDELINE FOR PHARMA
WHO GMP GUIDELINES
IF YOU HAVE ANY QUESTION ASK US ON THIS BLOG

Following are some of articles which;will be useful for you in further understanding of aspects of sterile dosage form manufacturing

FDA guidelines

What is 21 CFR PART 11

What is HEPA filter

Pharmaceutical Validation


Clean Room Classification


Pharmaceutical Industry


Pharmaceutical Manufacturing


Clinical Trials
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What is What is 510(k) Clearances ?
What is 510(k) Clearances, Premarket Notification for medical devices - PMN or 510(k)

What is an antibody? what is monoclonal and polyclonal antibodies?


Enzyme linked immunosorbent assay ELISA

Raido Immuno assay

http://whoguideline.blogspot.com/2010/04/terminalogy-and-their-explanations.html

Pharmaceutical Aseptic Manufacturing Process Terms , Terminology and Definitions.

http://whoguideline.blogspot.com/2010/02/pharmaceutical-aseptic-manufacturing.html

Here are some articles which will be useful for you in further understanding of aspects of sterile dosage form manufacturing and regulatory affairs and good manufacturing practice in pharmaceutical industry

Pharmaceutical Validation

Types of validations in pharmaceutical manufacturing


Requirements of documents for validation of sterilisation process

How to investigate OOS out of specification results

Determination of Phenol coefficient of a disinfectant

Sterility testing

Clean Room Classification

Time limitations in sterile pharmaceuticals processing

Aspects of validation of manufacturing process in sterile pharmaceuticals

Clinical Trials

Controlling Pyrogens in injectable dosage forms

Media fill run process simulation aspects Validation of Aseptic Process and Sterilisation

New Drug Application (NDA) how to make a New Drug Application (NDA) to US FDA

Abbreviated New Drug Application (ANDA) What is ANDA , detaied information about ANDA preparation and submission to US FDA

How to make Investigational New Drug (IND) Application to US FDA

Drug applications submission to us fda Over the counter Drugs OTC drugs

BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS

Electronic record in pharmaceutical manufacturing industry

Good manufacturing practice in pharmaceutical industry

Pharmaceutical industry pharmaceutical companies and FDA latest updates

Here is an interesting article on world wide pharmaceutical industry
Article on Pharmaceutical Industry pharmaceutical industry

Here are some interesting articles on Quality assurance systems for pharmaceutical company
1.Quality assurance in pharma industry

2.Quality by design concept for pharmaceutical industry

3.Quality by design concept in pharmaceutical industry an  explanation

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

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