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Tuesday, July 22, 2008

Pharma Water System Validation

All pharmaceutical water systems delivering Purified Water, Water Highly Purified or Water for Injection must be validated to demonstrate that they meet, and will continue to meet, their quality specification as laid down in the monographs of the relevant pharmacopoeias (USP or EP/PhEur), their requirements, as laid down in the User Requirement Specification (URS) and the requirements of the ISPE Baseline Pharmaceutical Engineering Guide.

water system validation we have a range of knowledge and experience which is seldom available within individual manufacturing companies.
aim is to provide a comprehensive validation service which ensures regulatory compliance is achieved quickly and cost-effectively, ensuring full traceability.
Prospective Validation for New Pharmaceutical Water Systems

Development of Validation Master Plan (VMP) and User Requirement Specification (URS)
Design Qualification (DQ)
Installation Qualification (IQ)
Operational Qualification (OQ)
Performance Qualification (PQ) - All Phases
conduct chemical and microbiological testing for the PQ1, PQ2 and introductory PQ3 phases
On-Going Monitoring Regimes (Continuous Compliance Assurance or CCA)
Validation Review
A Retro-validation exercise to determine the condition of the system

The production of protocols and the re-validation of the system ensure that any changes made to the system are captured and that the system is inspection ready

Change Control
Inauguration of a change control procedure to ensure compliance of any system change

Retrospective Validation for Existing Pharmaceutical Water Systems

The industry is required to maintain water systems in a validated state, operating under proper procedures with full water system documentation, maintenance and management control, that is supported by an appropriate monitoring regime.

Pharmaceutical Validations
There are occasions, especially if there have been system modifications or alterations, when it is necessary to carry out a retrospective validation. Unlike generic validation houses, which lack industry specific knowledge and assess the water system against today's standards and criteria (often resulting in unnecessary system re-build and expense), our approach is to evaluate the system according to its age and design principles and retrospectively validate only to critical parameters.

If you have any question for WHO GMP GUIDELINES ,WHO GUIDELINE ,you can write me on this website.

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

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Pharmaceutical Validation

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Pharmaceutical Industry

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


Unknown said...

Need advice on PQ - the phases & their Duration

Unknown said...

need an advise on pq the phases and their duration and microbiological test to be done

Unknown said...

need to clarify the criteria for retrospective validation for existing water system

Unknown said...

need to clarify the criteria for retrospective validation for existing water system

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