Validation Master Plan, Validation Plan and Matrix.

Validation VMP's, VP's and Matrix.

The VMP along with the Matrix, carries the complete overall picture of the companies validation activities, it enables a regulator to quickly assess, strengths and weaknesses and gauge where his time will be best spent. These are the most important validation documents. In it, are detailed the means and methods the company are using, and will continue to use, to conform to all cGMP guidelines and requirements. The VP document details how projects involving new, and or, updated equipment, will be integrated into production within the companies regulatory controlled quality environment.

   
Validation Documentation Matrix
$66.00  £33.40
667655
This Matrix must sit along side your VMP or PVP and together with these documents give a very concise overall picture of your validation program. This four part matrix allows you to list all the equipment and systems that must be qualified. Each entry is allocated a row in the matrix. The row consists of eleven headings, these may be edited as required (but come with all the standard documentation titles inserted). In this matrix there is room to enter the document number, prefixed by, A to D. The document number gives you the instant cross reference to the current document, the A to D prefix shows the progress stage.
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Validation Plan
$87.00  £44.02
890001
This document follows our well developed method of using a generic document and allowing the customer to apply an attached detailed SOP to it, turning the generic document quickly into a first class company bespoke document. This VP details and integrates all validation activities and procedures required for a small to medium sized project, involving production/facility/utility equipment using electronic controls or monitoring.
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Validation Master Plan
$87.00  £44.02
901000
This document follows our proven practice of supplying a generic document frame with an automatic method of populating it. Once populated, all you are required to do is follow the attached SOP as it takes you through a process section, by section, that changes your generic document into a detailed, referenced, bespoke company document. The document follows our three level URS system that ensures functionality traceability from the URS to the various testing protocols. A great document to author and use. This document interfaces with our Risk impact assessment (RIA), Validation Project Plan (VP), User Requirements Specification (URS), giving a seamless flow from Corporate Practices and Procedures - VMP - VP - IQ - OQ - PQ, while integrating flawlessly with the URS - DQ - RIA.
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