How to write a superb Validation Risk Assessment
Validation Risk Assessment 8946Knowledge of how to write a superb Validation Risk Assessment is an essential attribute when it comes to condensing three documents into one. 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 VraP document becoming notably easier to use and quicker to review and edit. This new format will make a very significant difference to the man hours required to produce and execute the Validation risk assessment ra 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 older style VP, VRA, & URS. Seamlessly integrating with this Validation Risk Assessment Plan is our equally new 4Q Protocol, which integrates the DQ/IQ/OQ/PQ into one document. This 4Q document is an essential step forward for companies seeking to reduce validation costs without sacrificing regulatory compliance.
VrrP + 4Q = FDA Compliant qualification.
4Q Equipment Protocol.
Validation Risk Assessment 7950The Equipment Validation risk assessment Plan has been designed specifically to replace the four standard protocols. By taking the contents of these four protocols 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 Validation Risk Requirements Plan (VrrP). 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 prefaced with a 10 page SOP containing detailed step by step instructions for you to use in in converting this interactive template into your own bespoke company document. For the end users convenience it is still written in MS word.
Understanding how to write a superb Validation Risk Assessment.
Validation Risk Assessment 1387This quite revolutionary two document package is all that is required to fully validate; to cGMP standards, equipment used in a 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 SOP’s 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 package are; not only unique, but also highly cost effective and intuitive to use. Each document is preloaded 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.
VALIDATION RISK ASSESSMENTS PLAN.
21 Years of retailing cGMP - 35k templates supplied to the industry.
01200002_VrrP_Equip_ Iss-4. $299.00
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.
12000006_4Q_Equip_iss-4___$299.00
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.
12000008 4Q Equip-Package.
$499.00
This quite revolutionary two document package is all that is required to fully validate; to cGMP standards, equipment used in a 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 SOP’s 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 package are; not only unique, but also highly cost effective and intuitive to use. Each document is preloaded 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.