EMPLOYEE APPRAISALS.


This graphic represents Toronto city skyline home to employee appraisals users.and tHIS GRAPGIC OF tORONTO SKYLINE IS USED IN eMPLOYEE aPPRAISAL


Introduction

Employee appraisals requires a methodology that in a relatively simply and clear format can measure an employee’s ability to perform in their current role and equate this ability to a numeric value that will then enable meaningful peer comparisons to be made.  This then enables management to see past first impressions and gauge the worth of an employee and assess their suitability for continuing employment or promotion within the company.   


From the UK.

Alarming Reports No. 2. - GPs have been warned over their vaccine storage systems after 813 patients at three practices in Aberdeen received damaged immunisations. NHS Grampian has launched an investigation after staff noticed vaccines were being stored in a defective fridge, at temperatures outside the range recommended by the manufacturers. Practice records showed 404 children and 409 adults were given the damaged vaccines between October 2004 and October this year. Dr Helen Howie, consultant in public health medicine at NHS Grampian, said: 'Vaccines may not have been consistently stored between the manufacturers' recommended temperatures of 2°C and 8°C. Therefore it is not possible to be certain that vaccinations administered at during that time will have provided full protection.' Experts called for closer scrutiny of what is a 'huge issue for general practice'. Dr Brian Crichton, a GP in Solihull who has conducted research on vaccine storage, said: 'We need to look at this as a serious issue. 'Efficacy can drop quite rapidly if medications or vaccines are left outside the recommended temperature range.' Affected patients have been offered booster vaccinations and all other vaccine storage fridges in Grampian practices are being examined for faults. Employee Appraisals.

CMP Information Ltd 2005


EMPLOYEE APPRAISALS.


Validation Risk & Requirements Plan (VrrP)
$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. 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.

VrrP+4Q Equip=Compliance

Quantity

4Q Equipment Protocol.
$299.00

This new 4Q Equipment Validation Protocol (4Q-Equip) has been designed specifically to replace four standard protocols. By taking the contents of the these four protocols and carefully weaving them into one notably easy to use protocol,  we have made significant progress in reducing validation paperwork.  Reductions of up to 75% have been quoted as the likely total. Integrating the old style DQ/IQ/OQ/PQ protocols into one 4Q document will be an enormous savings in man hours in the authoring, reviewing, updating and approving tasks. With the simultaneous introduction of the new Validation risk & Requirements Plan (VrrP) which integrates the VP, VRA & URS into one document - equipment validation has been reduced to two document.

VrrP+4Q Equip=Compliance

Quantity

4Q + VrrP Equipment Validation Package.
$475.00

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.

Quantity


 Package for Equipment Validation Level-2. (Issue 3) -- $585.00

During a regulatory visit the inspectors do expect to see a complete suite of validation documents in place for each validation task.  The use and scope of the individual documents has been documented, discussed and explained in detail.  It is therefore obviously best policy to have in place exactly what the regulator is looking for.  The use of a document packages ensures a multitude of regulatory requirements are catered for and possibly a similar multitude of pitfalls, blunders and omissions are anticipated and negated

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