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ALL DOCUMENTS ARE WRITTEN USING MS WORD OR EXCEL. THEY CARRY NO ADVERTS AND ARE 100% EDITABLE. WHEN YOU PURCHASE A DOCUMENT FROM THIS SITE YOU WILL AUTOMATICALLY BE SENT A URL LINK TO DOWNLOAD YOUR DOCUMENT. THESE URL LINKS ARE AROUND 130 CHARACTERS LONG AND IT IS ESSENTIAL THEY ARE NOT BROKEN.
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Available - COMBINED IQ/OQ/PQ:;      Available - LIMS Protocols and Packages:;      PROTOCOL AUTHORING DATA:      Available - AUTOCLAVE VALIDATION:      Get our - MONTHLY NEWSLETTER:     



VrrP & 4Q PLans and Protocols.

12000002_VrrP_Equipment_iss-4.
$298.00
12000002 Be the first one to write a review
This Validation, Risk & Requirements Plan (VrrP) is one document designed specifically to replace three. The contents of the three original documents were completely revised and edited into a more compact and interactive format. This new format will make a very significant difference to the man hours required to produce and execute these documents. There will also be a very noticeable reduction in the time required for the reviewing and approving tasks. This new document titled the VrrP replaces the VP, VRA & URS and now compliments our equally new 4Q Protocol, which integrates the DQ/IQ/OQ/PQ into one document. This is an essential step forward for companies seeking to reduce validation costs without infringing regulatory standards.

Quantity
12000006_4Q_Equip_iss-4.
$298.00
12000006 Be the first one to write a review
4Q Equip package has been designed specifically to replace four standard protocols. By taking the contents of the four protocol and carefully weaving them into one notably easy to use protocol, we have made a significant advance in the task of streamlining validation documentation by reducing protocol numbers by close to 75%. The new bang up to date 4Q protocol replaces the DQ, IQ, OQ & PQ and now compliments our equally new VrrP Protocol. By integrating the old style DQ/IQ/OQ/PQ into one 4Q document there are enormous savings in man-hours in the authoring, reviewing, updating and approving tasks. Start with a proven template that becomes bespoke as you edit it and finish with a professional cGMP compliant. Then you can face the regulators with confidence. For everyone's convenience, it is still written in word.

Quantity
12000008 VrrP-4Q-protocol-Package
$499.00
12000008 Be the first one to write a review
This is quite different from our usual validation packages, it is an evolutionary VrrP & 4Q protocol package comprising of only two documents that have been specifically designed to fully validate; to cGMP standards, equipment for use in a cGMP regulated facility. A lot of effort has gone into ensuring that repetitive instructions and actions have been designed out and innovative and intuitive risk-based methodologies have been incorporated. Both documents are prefaced with a methods' Standard Operating Practice (SOP) document. These SOPís lead you through the task of converting these highly detailed templates into your very own company bespoke protocols. The hyperlinks and cross-references within the VrrP & 4Q protocol package package are; not only unique but also highly cost-effective and intuitive to use. Each document is pre-loaded with the test scripts (complete with acceptance criteria). All test and inspection scripts are written in MS word, to facilitate simple editing of text, layout, tables and schematics.

Quantity
12000012_VrrP-Computer_iss_4
$298.00
12000012 Be the first one to write a review
This Validation, Risk & Requirements Plan (VrrP) is one document designed specifically to replace three. The contents of the three original documents were completely revised and edited into a more compact and interactive format. Resulting in the document becoming notably easier to use and quicker to review and amend. This new format will make a very significant difference to the man hours required to produce and execute these documents. There will also be a very noticeable reduction in the time required for the reviewing and approving tasks. This new document titled the VrrP replaces the VP, VRA & URS and now compliments our equally new 4Q Protocol, which integrates the DQ/IQ/OQ/PQ into one document. This is an essential step forward for companies seeking to reduce validation costs without sacrificing regulatory compliance.

Quantity
12000016_4Q_Computer_iss_4
$298.00
Be the first one to write a review
4Q Equipment Validation Protocol (4Q-Equip) has been designed specifically to replace four standard protocols. By taking the contents of the four protocol and carefully weaving them into one notably easy to use protocol, we have made a significant advance in the task of streamlining validation documentation by reducing protocol numbers by close to 75%. The new bang up to date 4Q protocol replaces the DQ, IQ, OQ & PQ and now compliments our equally new VrrP Protocol. By integrating the old style DQ/IQ/OQ/PQ into one 4Q document there will be enormous savings in man hours in the authoring, reviewing, updating and approving tasks. For everyone's convenience, it is still written in word.

Quantity