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COMBINED IQ-OQ PROTOCOL.

Introducing the new COMBINED IQ-OQ PROTOCOL…………………….CLICK HERE TO GO TO OUR DOCUMENT STORE
New from Validation Online a combined IQ-OQ protocol. Designed to cover equipment in general and specifically laboratory type equipment, with or without embedded or programmable software. This is not a list of chapter headings. It is a fully detailed interactive IQ and OQ protocol.

Now you too can raise a competent Combined IQ - OQ protocol in matter of hours, and sometime even in minutes.
Combined_IQ-OQ_Issue-1 -- $125.00
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This Combined IQ–OQ protocol is a really easy and attractive document to use. It is prefaced by a 10 page SOP, which enables you to follow the SOP instruction and progressively (page by page) convert this fully detailed template into a superb Combinrd IQ-OQ 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.

Our unique design was developed by a team of pharmaceutical consultants working across the pharmaceutical, medical device and biotechnical industries. These consultants covered all the validation disciplines and collectively pondered long and hard to come up with a design that would be acceptable to all users and highly cost effective for companies.

Now this new combined IQ–OQ protocol brings a refreshingly simple and attractive approach for the industry professional, enabling them to raise professional quality validation protocols in a very efficient and cost effective manner.
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.

Our unique design was developed by a team of pharmaceutical consultants working across the pharmaceutical, medical device and biotechnical industries. These consultants covered all the validation disciplines and collectively pondered long and hard to come up with a design that would be acceptable to all users and highly cost effective for companies.

Now this new combined IQ–OQ protocol brings a refreshingly simple and attractive approach for the industry professional, enabling them to raise professional quality validation protocols in a very efficient and cost effective manner.

VALIDATION DOCUMENTS & PROTOCOLS.

The V chart shown below indicates the relationship between the various validation documents and protocols. It can be easily recognised that each of these documents and protocols play an essential role in the validation task. All these documents must be considered mandatory in the majority of instances.

Essential protocols and documents include, the IQ, OQ, DQ and the PQ, along with the essential VMP, VP, URS, VRA

COMBINED IQ-OQ


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