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Networks.
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Package Network Validation. (Issue 6)

$680.00
10001110
The complete chain of regulatory required documentation for the validation of an IT Network system. This Validation Package does not contain the VMP as network qualification will usually be included in the the master VMP or a VMP dedicated to computer controlled equipment and or systems. This package contains one of each of these documents:
VP, URS, DQ, VRA, IQ, OQ, PQ.
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Network Validation Plan.

$115.00
10001111
The Network Validation Master Plan, is the starting point for validation, and hence the most important validation document. It improves validation efficiency greatly by forcing all concerned to document, review, and discuss, the proposed methods and allotted responsibilities. It is an
expected document with the FDA, and a mandated document with the EU. While in the past network validation was more focused on functions of single user network systems, recently the focus has progressed into network infrastructure, networked systems and on security, authenticity and integrity of data acquired and evaluated by network systems.

Document Statistics

 Protocols = 1

Pages = 29 

Paragraphs = 688        

Lines = 1332 

Words =  5571 

 Characters = 36210

 Graphics = 12

 Size = 303 KB


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PI-URS
Network User Requirements Specification.

$115.00
10001112
The document that sets the standard, and specifies your Network requirements in a manner that ensures when a system or piece of network is selected, it will deliver the functions you want, it will have maintenance standards, it will have calibration records, it will have all the documents and records to enable successful validation to be completed. This document was designed to be used as a live
document up until the DQ is completed and approved. It uses three levels of URS, URS Level 1, 2 and 3, and is the only URS to guarantee traceability from the URS through to the final PQ and OQ functionality testing. This traceability is a mandatory requirement for Full Life Cycle Validation of Network systems that are the subject of predicate rules. It can be used on mechanical, electrical and software controlled, monitored or driven systems.

Document Statistics

 Protocols = 1

Pages = 27 

Paragraphs = 481         

Lines = 1374 

Words =  2563 

 Characters = 18021

 Graphics = 14

 Size = 302 KB


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Network Design Qualification.

$115.00
10001113
The Standard Operating Procedure attached to this generic network design qualification protocol, will chapter by chapter, take you through the task of raising a fully detailed document. The main body is split into fourteen tables, each one probing the design requirements and standards for the individual requirement. Safety and security along with user operability are very detailed. The document will lead you through all these design aspects allowing you to delete some you feel are not important to your equipment. It is an easy document to use and will ensure that you’re DQ’s are relevant, up to date and easy to execute. Practically all the requirements are in table form. Allowing fast and clearly presented results to be obtained.

Document Statistics

 Protocols = 1

Pages = 29 

Paragraphs = 634        

Lines = 1961 

Words =  3142 

 Characters = 19475

 Graphics = 19

 Size = 316 KB


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Network Validation Risk Assessment.

$125.00
10001114
The Risk and Part 11 Validation Risk Assessment (VRA) protocol is becoming the most important document in the validation train. The VRA reassures the regulators that you have looked at specific network functionality and considered the appropriate level of validation that is required. You have also considered various aspects of its use and the implications of any malfunctions. From the results of this exercise the scope of all validation activity can and must be justified. This is a robust and simple to execute document, one that will lead you through the process and
deliver a result that can be used as the foundation for your validation activities. This VRA now includes the assessment table for categorising and documenting the new 21 CFR Part 11 guidance ruling on what predicate data must be stored in a Part compliant system, along with the new broadsheet to establish your new database of part 11 records. (now mandatory).

Document Statistics

 Protocols = 1

Pages = 18 

Paragraphs = 3440       

Lines = 810 

Words =  3110 

 Characters = 20080

 Graphics = 10

 Size = 179KB


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PI-IQ
Network Installation Qualification.

$115.00
10001115
Installation Qualification (IQ) is an important step in the overall validation and qualification process for software and networked systems. Our protocol leads you through the detailed requirements. GAMP 4, is used as a general guide, however there are some areas where it is better to stick with the FDA interpretations. Validation Online has extensive validation experience, where we know that there is a regulatory sensitive area we make absolutely certain that our documentation is clear, concise and supplies the information the regulators are anticipating. These protocols have evolved over 15 years use in the pharmaceutical and allied industries.

Document Statistics

 Protocols = 1

Pages = 51 

Paragraphs = 1030     

Lines = 3240 

Words =  6006 

 Characters = 38541

 Graphics = 39

 Size = 581KB


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Network Operational Qualification.

$115.00
10001116
Execution of the Network Operational Qualification (OQ) will verify that; Radio Frequency Interference. Application Software Identification. 21 CFR Part 11 Conformance Verification. Network Function Test. Safety / Health / Environmental Assessments. Security of Back-up Software. Power failure Test. System Documentation (SOP Verification). Operating System Software. Test Equipment Calibration. 21 CFR Part 11 Eligibility Verification.

Document Statistics

 Protocols = 1

Pages = 40 

Paragraphs = 664      

Lines = 2291 

Words =  4571 

 Characters = 28586

 Graphics = 23

 Size = 397 KB


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Network Performance Qualification.

$89.00
10001117
The Network Performance Qualification is the culmination of the validation process. The protocol is used in conjunction with the system operating SOP, to verify that the system process is consistent and correct. The results of the testing must be recorder and reviewed with a view to ensuring that the deviancies (within permitted tolerances) that exist are random and not a trend that will lead to out of specification operation during production use.

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