ISO 9001:2008 Quality Plan ISO 9001:2008 Quality PlanEfficient QMS™ - Simplifies Quality | Efficient QMS™ Lite Document Management System with Extraordinary Benefits
Typical Expenses for ISO 9001 Registration
Click here to browse the Starter ISO 9001 Quality Plan, $127. To aid transition to ISO, the procedures and forms that are referenced by the quality manual and management procedure can be used as place-holders for existing Company documents. The starter kit is useful to help management fully understand the scope of an ISO quality improvement project. The starter quality plan contains quality manual, conformance checklist, management planning and employee orientation tools to introduce a business to ISO 9001. We credit purchase of this kit after purchase of the Lean or Comprehensive kit - no time limit.
Click here to browse the ISO 9001 Bare Minimum Kit, $197 for businesses that don't want any more documents than necessary to achieve certification to the ISO 9001 standard.
Click here to browse the Lean ISO 9001 Quality Plan, $297. The Lean Kit presents a more mature business operation. The Lean ISO 9001 quality plan kit does not contain the "Value-Added" documents that are in the comprehensive kit. The lean ISO 9001 kit is designed to enable new businesses and less mature Companies to quickly earn their QMS pedigree.
Click here to browse the Comprehensive ISO 9001 Quality Plan, $397. The Comprehensive ISO 9001 QMS kit has more documents because of lessons-learned and continuous improvement opportunities that we've encountered over a significant time (30 years with the most demanding Customers on the planet). The additional forms and work instructions help to present a mature quality management system to increase credibility and earn more points from Customers - more points usually means more business.
At-PQC™ is an "open-book" website where you can browse the entire content of all demonstration documents, which means you will never take a chance with our products and guarantees you will make a well-informed decision about the right quality plan for your project. Tailor documents to display your business name and logo because the documents you download are fully editable in with MS Office or compatible program.
At-PQC™ demonstration documents are WYSIWYG; that is, what you see in demonstration documents is precisely what you receive in editable MS Office format and we don't impose invasive DRM User-limitations. Please use documents for your project according to license terms and conditions.
Email or call for assistance - no-charge Consulting by phone or email.
Get the free Adobe Reader to evaluate our demo docs.
Click here for tips to implement an ISO 9001 quality management system
Click here for a list of minimum ISO 9001 quality assurance requirements
Tailor the ISO 9001 quality plan policies, procedures and forms to meet your needs and use them according to license terms and conditions.
If you only need an ISO 9001 quality manual, please click here to evaluate the styles we offer.
Get the free Adobe Reader to evaluate our demo docs.
The ISO 9001 quality plan recognizes and employs basic rules:
the Customer establishes the meaning of quality...
if measurements are not performed then improvements cannot be made...
do it right the first time...
The ISO 9001 quality plan process approach can be simplified by stating:
continuously improve…
create partnerships with Suppliers...
focus your business on Customer satisfaction...
make decisions based upon factual measurements...
provide leadership and steering...
share the vision, objectives and plans with everyone...
structure the organization to work in a natural process flow...
systemize the processes to meet Customer requirements...At-PQC™ can help you implement the principles of the ISO 9001 quality plan by providing an effective and efficient business infrastructure that focuses on Customer satisfaction and continuous improvement. At-PQC™ can enable your business to realize desirable cost savings using practical business tools that focus on profit and growth.
Click here to learn more about QC principles
is the Username to open demo docs
Typical implementation strategy:
1) Management Buy-In...
Requires the business owners to take part in reviewing and guiding the system. The owners must rate their acceptance in ascending order from 'buy-in with resources' to 'participation' to 'leadership' to 'evangelism'. If acceptance ranges from 'negativism' or 'apathy' or 'tolerance' or 'verbal support' then there is no chance to economically transition.
2) Create or Modify the Business Plan to Integrate the System...
This is the next most important step in creating an environment or culture that will meet or transition to ISO 9001 quality plan on the first attempt. The existing business plan needs to be amended by the owners to incorporate an ISO 9001 quality manual to provide for its most costly or time-consuming features. The owners need to agree on the content of the plan for use by the Company.
The "what-to-do" functions to integrate the manual need to be addressed in the business plan, then the "how & when-to-do" functions become the workload for the Company. The plan needs to define the operations that will be excluded from the transition process.
Time: approximately 40 hours to release an initial draft of the business plan
3) Produce 3 Basic Documents Essential to Conformance to ISO 9001: Vision, Strategy to Achieve Company Objectives and Policies...
The Vision is the basis for all aspects of the Company's business plan. Operational plans become the basis for achieving the Vision, which assignment, involvement, commitment and responsibility. The strategy must include the ISO 9001 implementation plan, identification of required resources and measurements for success.
4) Select the Leaders to Produce a Tentative Implementation Schedule, Define the Cost of Implementation and Develop an Initial Implementation Plan...
Time: approximately 3 months
5) Evaluate Current Conformance...
Make team assignments, collect documentation and compare them to ISO 9001 quality plan requirements. This step is intended to organize and train teams and individuals to perform multi-functional shortfall analyses. This step involves many employees (almost everybody).
6) Determine the Shortfalls...
Assess procedural adequacy, identify gaps and omissions and scope tasks and resources. This step permits the evaluation of compliance variances and proposed remedial actions and then it deals with the organization of the results for the final implementation plan.
This step involves many employees (almost everybody).
7) Finalize the Implementation Plan...
Define tasks and assignments, schedule actions and employ a rigorous work discipline. This step covers all of the project management activities associated with the development, organization and scheduling of the final implementation plan, including all the factors that will make the plan succeed. This step involves few employees (5% to 15% of the workforce).
8) Define the Documentation Process...
Develop a documentation structure, a document control system and a writing-review process. This step examines ISO 9001 quality management system documentation activities, including its structure, purpose, usefulness and how to assure user ownership, as well as the factors that contribute to developing satisfactory documentation. This step involves functional management (up to 50% of the workforce).
9) Refine the Implementation Activity...
Involve users, conduct awareness training and assure usability of procedures. All employees must know the policy's content and how their assignment supports its achievement. This step examines how to achieve the new responsibilities and roles expected of management and employees. This step involves functional management (up to 50% of the workforce).
10) Perform an Internal Compliance Audit...
Documentation versus performance - internal audit structure - prepare for the Registrar. This step involves users and management efforts to develop, implement and document compliance verification activities. This step involves multiple functions and intensive auditing (15% to 20% of the workforce).
11) Perform Registrar Audit...
Close corrective actions and demonstrate compliance. This step provides the methods for selecting a Registrar, defines how to deal with the audit process, handles audit activities and responds to Registrar audit findings. This step involves facilitation of the Registrar (5% to 15% of the workforce).Click here to learn more about QC principles
Starter ISO 9001:2008 Quality Plan Kit, $127
Add ISO 9001 Starter Kit to Cart - instant download | View Cart
The starter kit is the lowest cost approach to obtaining the necessary skeleton of documents to establish an ISO 9001 quality plan. Use the references to procedures and forms in the quality manual as placeholders if your business already has sufficient documents to transition to ISO 9001.
Kit contains quality manual, conformance checklist, management planning and employee orientation tools.
Use the Design quality manual in the starter kit if your business designs and produces or manufactures its own products.
Use the Build-to-Customer requirement quality manual if your business produces products or manufactures according to Customer contract.
Use the Service quality manual if your business provides a service such as installation, maintenance, management, GSA contractor - or other non-manufacturing business operation.
Select your manual then archive the remaining manuals. The differences between the different style manuals are the exclusions listed in paragraph 3.2 and applicable paragraph numbers.
We credit purchase of the Starter kit after purchase of the Lean or Comprehensive kit - no time limit.
Use the following Username and Password to open demos.
To open docs, input at least once, the following Username and Password:
QMS-00 Design Quality Manual
QMS-00 Build-to-Customer Spec Quality Manual
QMS-00 Service Quality Manual
Changes in ISO 9001:2008
Action Item
Action Plan
Impact Analysis
Internal Audit Schedule
Internal Auditor Training slides included in kit
Introduction to QMS
Management Procedure
Management Meeting Report
Process Orientation Checklist
Quality Systems Assessment (in download)
Schedule to QMS Registration (in download, pro-rate dates as required)Starter ISO 9001:2008 Quality Plan Kit, $127
Add ISO 9001 Design Starter Kit to Cart - instant download | View Cart
Bare Minimum Kit, $197
Add Bare Minimum Kit to Cart | View Cart
If your business builds to Customer requirements then use the "Build-to-Customer Spec Manual" and archive the Design and Service manuals and design related procedures and forms.
If your business provides a service then use the "Service Manual" and archive the Build-to-Customer Spec and Design manuals and calibration procedure and design related procedure and forms.
If your business designs its own products then use the "Design Manual" and archive the Build-to-Customer Spec and Service manuals.
QMS-00 Design Manual
QMS-00 Build-to-Customer Spec Manual
QMS-00 Service ManualSeventeen (17) Required Procedures. Numbers in parentheses are from the ISO 9001 standard.
All of the following documents are applicable if your Company designs its own products.
Calibration (7.6 may not be applicable for service business)
Configuration (7.3.7 may not be applicable for service business)
Contract review (7.2.2)
Control of documents (4.2.3)
Control of nonconformances (8.3)
Control of records (4.2.4)
Corrective and preventive actions (8.5.2, 8.5.3)
Design development (7.3.4 may not be applicable for service or build-to-spec business)
Internal audit (8.2.2 - quality system assessment and auditor training slides in download)
Management review (5.6)
Production and service (7.5.1)
Purchasing (7.4)
Receiving (7.4.3)
Responsibilities and authority (5.5)
Shipping (7.2.1, 7.5.1, 7.5.5)
Training (6.2.2)
Validation and verification of processes (7.1, 7.3.1, 7.3.6, 7.5.2 - included in design development procedure)Nineteen (19) Required Records. Numbers in parentheses are from the ISO 9001 standard.
All of the following documents are applicable if your Company designs its own products.
Calibration (7.6 may not be applicable for service business - additional forms in download)
Contract review (7.2.2)
Corrective action (8.5.2)
Customer property (7.5.4 - additional forms in download)
Customer satisfaction (5.2, 6.1, 7.2.1, 8.2.1, 8.4 - additional form in download)
Design and development change (7.3.7 may not be applicable for service business)
Design and development inputs (7.3.2 may not be applicable for service business - same form as development change)
Design and development review (7.3.4 may not be applicable for service business)
Design and development validation (7.3.6 may not be applicable for service business)
Design and development verification (7.3.5 may not be applicable for service business - same form as validation)
Identification and traceability, if required (7.5.3 may not be applicable for service business - additional forms in download)
Internal audits (8.2.2)
Management review minutes (5.6.1)
Monitoring and measurement (8.2.4 - additional forms in download)
Nonconformances (8.3 - additional forms in download)
Preventive action (8.5.3 - same as corrective action form)
Planning of product realization (7.1 - same as design and development change)
Supplier evaluation (7.4.1)
Training (6.2.2 - certificates, logs and request form in download)
Validation and verification of processes (7.1, 7.3.1, 7.3.6, 7.5.2)Bare Minimum Kit, $197
Add Bare Minimum Kit to Cart | View Cart
Lean ISO 9001:2008 Quality Plan Kit, $297
Add Lean ISO 9001 Kit to Cart | View Cart
The Lean Kit presents a more mature business operation. The lean ISO 9001 quality plan kit does not contain the "Value-Added" documents that are in the Comprehensive Kit.
Use the Design quality manual in the starter kit if your business designs and produces or manufactures its own products.
Use the Build-to-Customer requirement quality manual if your business produces products or manufactures according to Customer contract.
Use the Service quality manual if your business provides a service such as installation, maintenance, management, GSA contractor - or other non-manufacturing business operation.
Select your manual then archive the remaining manuals. The differences between the different style manuals are the exclusions listed in paragraph 3.2 and applicable paragraph numbers.
Click on the following links to evaluate the contents of the lean ISO 9001 design quality program kit, which you can use in your business operation according to license terms and conditions.
We credit purchase of the Lean kit after purchase of the Comprehensive kit - no time limit.
The Kit contains all documents listed below.
Use the following Username and Password to open demos.
To open demo docs, input at least once, the following Username and Password:
QMS MANUAL and PROCEDURES
QMS-00 Design Quality Manual
QMS-00 Build-to-Customer Spec Quality Manual
QMS-00 Service Quality Manual
QMS-01 Document Control
QMS-02 Configuration Management (required to control modifications to specs and drawings)
QMS-03 Records Control
QMS-04 Management
QMS-05 Responsibilities-Authorities
QMS-06 Training
QMS-07 Proposal Development and Contract Review (quality plan for scheduling and integrating project milestones)
QMS-08 Purchasing
QMS-08-1 Purchase Order Review
QMS-09 Receiving
QMS-10 Production
QMS-11 Shipping (when applicable)
QMS-12 Internal Auditing
QMS-13 Corrective and Preventive Action
QMS-14 Control of Nonconformances
QMS-15 Calibration (when applicable)
QMS-16 Definitions and Abbreviations
QMS-17 Design and Development (when applicable)
QMS Introduction
QMS System Overview (brief overview to provide to Customers or proposals)FORMS and WORK INSTRUCTIONS
8-Step QMS Implementation in download
5 S's in download
Action Item
Action Plan
Bulletin (multi-purpose change control document - very useful when signed by CCB Members - see QMS-02)
Calculated Risk Release
Calibration Reference Only Tag
Calibration Seal
Calibration System Forms
Certificate of Compliance-1
Certificate of Compliance-2
Compliance Matrix-1
Compliance Matrix-2
Contract Review Forms
Corrective Action Request
Customer Perception Survey
Customer Satisfaction Survey
Daily Receiving Log
Dimensional Analysis-1 (when applicable)
Dimensional Analysis-2 (when applicable)
Dimensional Analysis-3 (when applicable)
ECP (Engineering Change Proposal, Mil-Spec)
Engineering Order Form (EO)
Final Inspection Tag
First Article Inspection (AS9102 compliant procedure and forms in download, when required)
First Article Instructions (when applicable)
First Piece Inspection Report (when applicable)
Good Material Dot, Peel-and-Stick
Good Material Tag, Dock-to-Stock
Good Material Tag
Information Request
Inspection Instruction (form to detail onsite inspections)
Inspection Record (form to record results of onsite inspections)
Inspection Report (revise as required to summarize onsite performance)
Inspection Summary (alternate form in download)
Inspector Stamp Log
Internal Audits in Download:
Corrective and Preventive Action
Design and Development
Internal Auditing
Management
Production
Proposal Development / Contract Review
Purchasing
Receiving
Shipping
Internal Audit Form
Internal Audit Progress Report (in download)
Internal Audit Schedule
Internal Auditor Training Slides in download
Management Meeting Report
Nonconformance Report, RFS (alternate styles in download)
Packing Slip (CofC)
Procedure Template-1 (form to document project requirements)
Procedure Template-2
Procedure Template-3
Process Orientation Checklist
Production Inspection Record-1
Production Inspection Record-2
Production Readiness Review
Property Certification from Supplier
Property Control Tag
Property Management Log
Property Record
Purchase Order
Purchase Requisition
QC Tags-1
QC Tags-2
QC Tags-3
Quality Systems Assessment in download
Receiving Hold Dot
Receiving Inspection Instructions
Receiving Inspection Record
Receiving Log
Request for Change
Returned Goods Disposition Form (when applicable)
RFW-RFD, Commercial (request for waiver-deviation)
RFW-RFD, Mil-Spec
Routing Ticket-1
Routing Ticket-2, Peel-and-Stick template
Routing Ticket-3, Peel-and-Stick template
Routing Ticket-4
Schedule to QMS Registration (pro-rate dates as required)
Shelf Life Expiration Log (when applicable)
Shipping Log (when applicable)
Supplier Evaluation (demonstrate control of Suppliers, mail-merge list in download)
Supplier Performance Rating (mail-in form)
Supplier Performance Rating Spreadsheet (mail-in spreadsheet form)
Supplier Quality Requirements (flowdown to Suppliers)
Supplier Rating Cover Letter
Supplier Survey
Training Certificate-1
Training Certificate-2
Training Log
Training Matrix (for QMS procedures)
Training Orientation Request
Training Program Progress Report (included in download)
Trend Chart, Customer Satisfaction Chart, Grand Avg
Trend Chart Customer Satisfaction Chart, Individual
Validation-Verification Form (when applicable)
Withhold Tag
Work Instruction-1 (form to detail onsite work activities)
Work Instruction-2
Work Instruction-3
Work Instruction-4
X-Bar & R Chart (when applicable)
Zero Acceptance Number Sampling Plan (when applicable)Lean ISO 9001:2008 Quality Plan Kit, $297
Add Lean ISO 9001 Kit to Cart | View Cart
Click on the above links to evaluate the contents of the ISO 9001:2008 Quality Plan Kit, which you can use in your business operation according to license terms and conditions.
Comprehensive ISO 9001:2008 Quality Plan Kit, $397
Add Comprehensive ISO 9001 Kit to Cart | View Cart
The comprehensive kit contains all the documents listed in the Lean ISO kit plus the following "Value Added Forms and Work Instructions". The comprehensive kit is for businesses that consistently use lessons-learned and key measurements to continuously improve, which needs a few more procedures and forms to accomplish than the Lean ISO kit.
Click on the following links to evaluate the contents of the additional documents in the comprehensive ISO 9001 quality plan kit, which you can use in your business operation according to license terms and conditions.
The Comprehensive Kit contains all documents listed in the Lean ISO kit plus those shown below. Use the following Username and Password to open demos.
To open demo docs, input at least once, the following Username and Password:
VALUE ADDED FORMS and WORK INSTRUCTIONS
Authorization to Ship-1
Authorization to Ship-2
Certificate of Origin-1
Certificate of Origin-2
Certificate of Test-1
Certificate of Test-2
Chemical ID Tag
Configuration Audit
Cost of Quality
Data List, Drawing Tree
Drawing Template, Size "A"
General Requirements
Impact Analysis
Invoice and Packing Slip
Job Sheet
Material Certification-1
Material Certification-2
Metrics
MSDS
Product Release Record-1
Product Release Record-2
Request for Change
Requisition for Stock Controlled Goods (Materials)
Statement of Work
Trend Chart, Delivery Rating (individual rating in download)
Trend Chart, Nonconformances
Trend Chart, Yield Rating (individual rating in download)
Validation of Tools and Molds
Validation Plan
Variation Management of Key Characteristics
Warranty Product Review Report
Warranty Service Review ReportComprehensive ISO 9001:2008 Quality Plan Kit, $397
Add Comprehensive ISO 9001 Kit to Cart | View Cart
The comprehensive kit contains all the documents listed in the Lean ISO kit plus "Value Added Forms and Work Instructions". Click on the above links to evaluate the contents of the Comprehensive Quality Plan Kit, which you can use in your business operation according to license terms and conditions.
- Efficient QMS™ -
Are you driven to convert your effective or undocumented QMS into an efficient quality management system to survive implementation and maintenance of standards like AISC, AS9100, AS9110, AS9120, ISO 9001, FAA FIS, FAA PMA, FAA Repair Station, Nadcap, USACE or other comprehensive QMS that you know is required to compete in today's world market?
Recent Questions from Customers:
We are a two person shop and need some help to quickly become compliant with a Customer requirement. Do you have something we can use?
We have 47 Employees and lots of Customers. One of our team members in a recent management review meeting suggested we find something that will simplify things. Can you help?
Our small business has used MIL-I-45208 for years but our local QAR just rotated to another person and he wants to change our contract to require compliance to ISO 9001. We can't afford to give an arm and a leg to get compliant with ISO and there's no time in our delivery schedule to implement all this stuff. We could renegotiate the contract but we don't want the hit to our ABVS score. We really need something that's easy to maintain and won't cost an arm-and-a-leg. Will your eQMS thing do the job?
We've got tons of records in storage and we're constantly adding to it. We recently learned it would cost us over $30K to transfer all of it back to our shop or dispose of it. We have got to do something to get out from under this baggage or $30K will become $100K in a couple of years. Management wants to go paperless but can't find a cheap enough solution. We've looked online but everything is way too expensive, then we saw your Efficient QMS program. Will it really work to help us go from paper to electronic records?
Most businesses don't have a lot of time to develop a quality system and would rather find something that is already done, easy to manage and compliant with Customer requirements.
Think of the advantages you'll have when you can remotely access Company policies, procedures, work instructions, forms and records or demonstrate for any Customer in realtime your commitment to quality.
See for yourself how you can access and operate demo Efficient QMS™ to browse what could be your quality plan and records using your Blackberry, iPad, iPod, Palm, Smartphone or any device with internet Browser software.
Type-in the following address in your portable device or click the following link with your computer to begin using eQMS:
http://www.as9100-quality-system.com/demo
User-friendly point-and-click operation. Any device with Browser capability can access and operate eQMS so you're never cutoff from your records or QMS policies, procedures, work instructions and forms, including other categories and business documents that you assimilate into eQMS. Efficient QMS™ quality plan software was developed to eliminate undesirable overhead expenses and labor-intensive QMS system maintenance.
Efficient QMS Web App is a simple, cost effective, cloud-based and paperless solution that simplifies management activities for any Company.
User-friendly point-and-click operation.
Does your business need a good set of tools that actually simplifies a modern-day quality management system?
Imagine a point-and-click working environment for a QMS where everybody logs in and is instantly familiar with how things work because it is internet-based.
Users can access QMS documents and fill out forms online using any device with an internet browser - that's any desktop, laptop, netbook, tablet, PDA, Blackberry, iPad/iPhone/iPod and smartphone - any device with an internet Browser.
Records are in a database so they don't have to be transposed to a spreadsheet to analyze and there are no transposition errors.
Action items are displayed as soon as a User logs in and they're all displayed on the Events Calendar. Plus, eQMS sends email notifications and reminders in advance to enable Users to maintain their commitment to the schedule.
The latest revision documents are just a click away and are never caught by an Auditor because they are never out-of-date.
Documents under revision and new documents are controlled through a release process that assures the current documents are used right up to the moment that new documents are released.
Auditors love eQMS because everything they need to substantiate compliance is a point-and-click away.
Customers can log-in using a built-in Customer account that only displays QMS procedures and blank forms to protect proprietary information.
eQMS is expandable to enable access to other Company resources.
Scanned or PDF documents can be attached/embedded in forms, such as certs, receiving reports, contract modifications, drawings and more... If documents are too large to attach or embed in a record then the User can create a link to display the document.
Video training guides are the only resources needed to learn how to use the features of eQMS and they can be expanded to train other Company activities.
Procedures and records can be sent "live" to Customers, Suppliers, Potential Clients and Users to browse or fill out without having to log-in to eQMS.
Any form in the Company can be created using Form Maker and any procedure can be imported and edited using Process Maker.
Forms can be signed by responsible authorities to assure approval to proceed and prevent assumptions.
If you're a small business with few employees and no QMS documents that must compete with large businesses that have a certified quality plan, please click here to learn more about the Efficient QMS™ software quality management system. If you're a medium-to-large business and must find a way to transition from paper to electronic management then please click here to see for yourself how demo eQMS will make that process less painful.
A QMS pedigree requires extensive resources and tools to achieve certification and significant overhead to maintain the system for annual recertification. eQMS was designed to achieve QMS certification using existing employees and significantly reduce or eliminate overhead expenses.
Are you faced with the challenge to increase revenues and think a QMS pedigree will improve your odds? Do your budget limitations force you to call upon your employees to implement and maintain a complex QMS standard with diminishing resources?
All our Customers consider eQMS a formidable tool in their arsenal of business resources to facilitate Company policy and keep "things" under control and continuously improving.
Efficient QMS™ is a self-contained resource that's accessible on your internal network or over the internet. Users can login to mine the data, sign authorizations, do homework, complete unfinished tasks, quote from the manual or procedures, access drawings and work instructions and demonstrate in realtime for your Customers how committed your Company is to quality. Your "office" is always open and your business files are always handy...!
From the Quality Manager of Electro Energy Inc:
"Efficient QMS™ helped us achieve a 99% score from our AS9100 certification audit and helped us maintain our QMS after being downsized. The Auditors from NSF-ISR remarked that our quality plan was in their top ten list of best practices."FYI: Electro Energy purchased the Eagle-Picher (EP) Colorado Springs, CO facility in Oct 2003 and transferred all personnel as assets of the sale. The QA Mgr had been with EP since March 1981 and most other personnel had as many years of experience in the business. Between 2003 and 2005 the Company became publicly traded. It took a couple of years for old management to retire then new management decided on Dec 1, 2005, to acquire an AS9100 pedigree. By July 7, 2006 the Company had its pedigree from NSF-ISR with a 99% score using Efficient QMS™ as the foundation of their quality management system. The QA Mgr knew the sale of EP to EEI would cause a paradigm-shift so he began to develop a web-based QMS in April 2004 to make the culture shock less painful, not to mention that EEI inherited over 30 years of document baggage that had to quickly become "auditable". The result of all this effort is Efficient QMS™.
Efficient QMS™ is a solution for companies that must protect their existing business and desire to compete for more business with Customers that want their Suppliers or Contractors to have a QMS pedigree - or operate with software-based project management tools.
We have very carefully created a browser-based working environment for management of simple or complex quality plans. We have succeeded in achieving the goal of operating a pedigree QMS without the need to hire additional personnel to maintain the QMS. In addition, eQMS Users are able to maintain a certified QMS when the business is victimized by down-sizing.
We designed Efficient QMS™ with emphasis on improving the management of Company resources and reducing the labor required to keep things up-to-date.
eQMS enables paperless management of:
- bulletins
- calibration
- changes
- configuration
- corrective actions
- expired materials
- forms
- improvements
- manuals
- policies
- procedures
- production records
- nonconformances
- preventive actions
- purchase orders
- receiving inspection
- training
- work instructions - and more...
Simple, low cost Efficient QMS™:
- has a daily planner with reminder login for Users that can't remember everything they need to do
- has a video User's manual
- has easy navigation for all Users with their internet Browser
- has flexibility to add or remove categories to fit the business operation - and more...
Click here to learn how-to add any word-processed document to Efficient QMS™.
We invented Efficient QMS™ out of self-preservation and it has saved countless hours of labor and significantly decreased "management" expenses. User's intuitively navigate eQMS because it is browser-based and because it is such a convenient tool to access QMS documents and records after password-protected login.
We recommend installation of eQMS on an external webhost to enable "road warriors" to manage their business in realtime using any device with Browser capability. Not a bad idea if you're sitting with a Customer talking shop and suddenly need to browse some records. Think about the intangible return on investment from increased Customer confidence in the business operation.
Anywhere you can connect to the internet or internal server to login to eQMS is another tool to promote and manage your business.
Click here for more information or click here for demo to vigorously experiment with eQMS.
We are proud Efficient QMS™ was chosen to support the quality improvement projects for the following services, businesses and agencies. Companies using eQMS have received pedigrees for ISO 9001, AS9100, AS9110 and Nadcap special processes:
Access Laser Company
Alto Aviation, MA (aircraft sound systems)
Arcadia Aerospace Industries Testimonial: "We went through our Nadcap audit for AQS and NDT/UT and we received no NCR's. The Auditor was very complimentary of our system, which was in no small part because of eQMS."
Avionics Mounts Inc.
axept Custom Engineering (MEMS)
Canadian Solar Solutions Inc. This manager started working for Canadian Solar Solutions shortly after setting up and operating eQMS for his previous employer, Sustainable Energy Technologies. Because of lessons learned at his old employer, he convinced new management to use eQMS to help them survive a CSA audit in six (6) weeks, which they passed.
Deutsch (.net) This global Company could route all their satellite businesses through one internet-based quality management system to standardize a critical business operation.
Dynamic Paint Solutions
Dynamic Power LLC
Global Parts Inc.
Howell Instruments Inc.
K-TECHnologies Inc.
Ligi Tool and Engineering Inc.
McAllister Tool and Machine
Midstate Industrial Supply
Mohr and Associates
Nee's Machine Inc.
Nomad Aviation Inc. Testimonial: "We passed our ISO 9001:2008 registration audit thanks to Efficient QMS...Thank you."
Quipco Al Shoumoukh, LLC
Sandia National Laboratories
Specialty Metals Corporation
Sustainable Energy Technologies
Theranos
Quest Manufacturing LLC. Testimonial: "Installing eQMS was very simple. The only issue we had with install on our server was getting the correct library for 64 bit and that was quickly cleared up."
Price - $497 - includes versions to support ISO 9001 or AS9100C, AS9110A, AS9120A or AISC. Other QMS systems available with prior notice, such as nuclear quality management.
The above demo links are useful to learn what is included in each download version of eQMS.
$497 Efficient QMS™, Complete | Add to Cart | View Cart
Efficient QMS™ software quality management system is accessible on any device with an internet Browser, including a WiFi enabled, private network webhost server. Click here for full-access demo to vigorously experiment with eQMS or click here to learn more...
Download and install fully functional Efficient QMS™ anytime on your webhost or internal server then we'll visit with you to provide a permanent license.
$397 Efficient QMS, Lite | Add to Cart | View Cart
Efficient QMS™ Lite is seeded with only a couple of documents to enable businesses to create their own proprietary management system or use it as an online document management system to manage important Company documents that need to be easily accessible to Employees or to replace paper forms with searchable electronic forms. Click here for full-access demo or click here to learn more... All the features in complete eQMS are included in Efficient QMS™ Shell.
Here's an interactive orientation video to quickly learn how to create a signature for use in eQMS:
New Features:
Ability to allow/disallow editing on data fields by the "customer/customer" login.
Ability to change the "customer/customer" login password.
Ability to change the encryption key used for generating the Customer Access Link to disable previously emailed links.
Allows signature authority Users to have multiple signature images. Signature Users can select a single signature or multiple signatures when "signing" a document.
Automatic document revision control and manual document release system. We originally only provided for revision control of forms.
Built in HTML editor. We originally did not provide for editing of procedures or work instructions within eQMS - an external editor was required.
Enhanced security.
Many bug fixes.
New Form Maker functions in the design palette.
New numerical data input types in forms.
Provide Form Maker database content to enable editing of all supplied forms. We originally did not enable editing of supplied forms.
Efficient QMS™ is not pay-as-you-go software - no subscriptions - no per-User fees - no other expenses - that's refreshing!
Evaluate eQMS to see how it can dramatically improve the efficiency of the quality plan that you need to keep your Customers happy. Any size business (including a one, two or three person shop or "big business") can use eQMS to help make the sale to win new business or keep costs way down for existing business. You'll never have to say "I'll get back with you on that..." because all you have to do is login to demonstrate in realtime the Company's commitment to "quality".
You can populate eQMS with any management system - including standards like AS9003, AS9100, AS9110, AS9120, ASA-100, ISO 9001, ISO 15161, MIL-I-45208, MIL-Q-9858, FAA-PMA, NQA-1, FAA Repair Station, TS16949 - and non-standard management systems like Construction, Maintenance, Machine Shop, Engineering, Commercial, Civil, Government - any Customer flowdown quality plan or voluntary quality management system!
How will your business spell relief?
Efficient QMS™
Insight to performing first article inspection FAI:
Characteristic Accountability
The Company shall verify and record the results of every design characteristic during first article inspection FAI. Every design characteristic shall have its own unique characteristic number.
NOTE: Reference characteristics may be omitted from the first article inspection FAI.
NOTE: Use more than one line if needed for any characteristic.
NOTE: Characteristics not measurable in the final product shall be verified by destructive means or during the manufacturing process (as long as they are not affected by subsequent operations). Characteristics verified at the detail level may be referenced in the assembly-level first article inspection report (FAIR).
Record of Results
Results from inspection of design characteristics shall be expressed in quantitative terms when a design characteristic is expressed by numerical limits. The Company shall record the results in the units specified on the drawing or specification unless otherwise approved by the Customer. Go/no-go data may be used when the design characteristic does not specify numerical limits (e.g., break all sharp edges) or an inspection technique is unavailable to provide quantitative terms. Go/no-go data may also be used when qualified tooling is used as a check feature for a specific characteristic.
Click here to go to the first article inspection procedure FAI.
Compatibility Guaranteed!
If you cannot edit our document(s) in your MS Word, Excel or Visio program we will fix it or refund your purchase.
Can't find what you're looking for...?
Please call, Fax or Email Us at:
Jennifer and Frank At-PQC™
JnF Specialties, LLC
664 Greenscape Lane
Colorado Springs, Colorado 80916
Cellphone Support: 719-649-4242Cellphone Support 6:00am to 6:00pm.
Fax: 719-573-4205Click here to bookmark At-PQC™ then visit our Toolbox to find a quality control plan that will help you achieve an effective and efficient business infrastructure that focuses on customer satisfaction, continuous improvement and desirable cost savings. Visit with us today for comprehensive assistance in developing or choosing the right quality control plan for your business. Click here for help with where-to-start.
Get the free Adobe Reader to evaluate our demo docs.
Here's how At-PQC™ can help you?
- Download editable documents for your project anytime...
- Tailor the editable documents to display your information...
- ...move-on to your next priority!
At-PQC™ demo documents are WYSIWYG, that is, what you see in our demonstration documents is precisely what you receive in editable format. This guarantees a well-informed decision for your quality improvement project. Documents can be downloaded immediately upon completion of an online transaction or selections can be delivered by email upon receipt of your purchase order at our fax number 719-573-4205.
At-PQC™ shares a commitment and passion to continuously improve. Our most sincere desire is to make a significant and positive difference in the lives of practitioners and business leaders that are responsible for the success of their business. At-PQC™ is committed to providing the highest possible level of technical documents for the support of quality improvement projects. We believe in the unlimited potential for continuous improvement and we're prepared to support any improvement project that you can imagine - welcome to At-PQC™.
Jennifer and Frank At-PQC™
JnF Specialties, LLC
664 Greenscape Lane
Colorado Springs, Colorado 80916
Cellphone Support: 719-649-4242Cellphone Support 6:00am to 6:00pm.
Fax: 719-573-4205
Visit with At-PQC™ about any aspect of your improvement project during your office hours.
Email At-PQC™:
We're here to support your ISO 9001 quality plan with our full attention and we know our website and experience will enable you to quickly and efficiently complete your ISO quality plan to proceed with the next action item on your list.
Home | ISO Service Kit | ISO Build-to-Print Kit | Sitemap | AS9100C | AS9110A | Contact | User Conditions |
At-PQC™ is a trademark and service mark of
