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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. Calibration of Humidity & Hygrometer Sensors.Humidity sensors require frequent calibration and continual monitoring, they are, along with pH sensors, the most prone to error sensors in general facility use. They should be calibrated against a range of Chemical mixtures that establish a specified humidity calibration level in small atmospheric containers. These chemical mixtures are issued with UKAS traceable humidity calibration certification. They are supplied in a kit that includes three certified standards covering the low mid and high sectors of the relative humidity calibration percentage range. The kit includes three ready to use enclosures (with certification of their values), a range of adaptors to suit your sensors, a sample FDA compliant calibration certificate and a complete detailed method statement on exactly what to do. All these items are contained in a robust neat and easy to handle carrying case. To read more or purchase your test kit please click on link below. 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.
It is anticipated that certain PC game consoles and accessaries will be sold out well before Christmas time. So, if your are intending to buy one:
THEN CLICK HERE NOW. Great Prices for - PS3 - Wii - DS1 - PSP and all accessories. GO TO:- VALIDATION ONLINE DOCUMENT STORE |