Our new combined IQ/OQ protocol has been a great success, with the majority of purchasers including a Validation Master Plan with their purchase of the IQ/OQ.  This is good but raises the question; what about the Validation Risk Assessment.  This is crucial to justifying the scope of your validation.  So to try and encourage the use of the VRA we have put  together a small package that includes the IQ/OQ / VMP / VRA documents for the condensed sum of $249.00,  (See below for purchase link).  This package is only available from this news letter. 
 
Now you too can use a very cost effective way of qualifying your laboratory equipment.

The
Combined IQ – OQ protocol has proved to be a really easy and attractive document to use. The ten page SOP that forms the preface renders the document extremely user friendly and allows swift and rapid transformation from an interactive template to a fully detailed and referenced, company bespoke protocol.

This protocol is targeted at equipment and is suitable for all equipment from the laboratory to the process line. All standard verifications are already included in the protocol format and all test scripts are fully documented and referenced.

Validation Online documents should never be confused with the routine document templates available on the internet. These templates are mainly little more than a list of chapter headings. Where as, Validation Online documents are of a unique interactive design which has been developed over the last ten years. Ten years during which regulatory compliant documentation has been successfully supplied to over sixty countries.

Combined_IQ-OQ_Issue-1 -- $125.00
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Combined IQ-OQ. VMP & VRA Package. -- $249.00
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Calibration of Humidity & Hygrometer Sensors.

Humidity sensors require frequent calibration to ensure they are not causing your Air Handling Units to over dry the air for your facility. This is a very common fault and can increase your energy costs by over 200%. It really is cost effective to calibrate in house.

The calibration kit arrives ready to use and only requires annual recertification. It is housed in a robust neat and easy to handle carrying case.

To read more or purchase your test kit please click on link below.

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Are you ready for an inspection?
With HEPA filters, the manufacturers recommended dirty filter change pressure differential (PD), is only correct if the filter is used at exactly the the same air flow as the makers specify. If there is any digression (there is often as much as 50% digression) then the makers PD must be corrected. If this is not carried out you can compromise the integrity of your room / machine pressure regimes. As you are no doubt aware this would be a very serious state to be in. There are also health and safety problems that can arise, if personnel are not getting the air flow protection that is sometimes designed into the system. This test script is not in the standard OQ, and is only available here as a download.  Regulators ask to review your writen justification for these filter change PD's; make certain you have them.
Purchase your copy of this test script now at Special Price of $16.00.
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The SOP for Equipment Validation continues to be an extremely popular document. This document leads you through the validation process, from the URS to the final P2Q.
Purchase your copy now at Special Price of $16.00.
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Click Here - To Download Your Own Free Pharmaceutical Glossary.



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