AS9120A
Complete Aviation, SpaceHome | AS9120A Starter Kit | Resources | Contact | User Conditions |
Click here to go to the Efficient QMS™ software program that converts your QMS into an efficient QMS.
Complete AS9120A Kit to implement the Aviation, Space and Defense Distributor Standard, $397 (formerly Stockist Distributor)
Add to Cart - instant download | View CartClick on the following links to evaluate the contents of the AS9120A aviation, space and defense distributor standard kit. If your business model does not include assembly or manufacturing then delete procedure numbers QMS-10 Production and QMS-17 Design and any reference to them in the quality manual.
Click here to learn about the purpose of a quality plan.
Please review our terms and conditions.
If you desire to register your QMS you will need to purchase the SAE sponsored document to support your project - please visit the SAE website to purchase the AS9120A and AS9121 standards:
http://www.sae.org/technical/standards/AS9120A
http://www.sae.org/technical/standards/AS9121Click here to get the latest free Adobe Reader to evaluate our demo docs.
is the Username to open demo docs
PROCEDURES - WORK INSTRUCTIONS
Internal Auditor Training
QMS-00 Quality Manual (rev "Orig" included at no charge)
QMS-01 Document Control
QMS-02 Configuration Management
QMS-03 Records Control
QMS-04 Management Process
QMS-05 Responsibilities Authorities
QMS-06 Training Program
QMS-07 Proposal Development and Contract Review
QMS-08 Purchasing
QMS-08-1 Purchase Order Review
QMS-09 Receiving
QMS-10 Production (if applicable)
QMS-11 Shipping
QMS-12 Internal Auditing
QMS-13 Corrective and Preventive Action
QMS-14 Control of Nonconformances
QMS-15 Calibration
QMS-16 Definitions and Abbreviations
QMS-17 Design and Development (if applicable)
QMS Introduction (for training)
QMS Quality Policy Handout
Zero Acceptance, C=0 Sampling Plan Table
Zero Acceptance Number Sampling PlanFORMS
Action Item
Authorization to Ship-1 (for product release provision if applicable)
Authorization to Ship-2
Bulletin (use for configuration control to document instructions for product release)
Calculated Risk Release (for product release provision if applicable)
Calibration System Forms
Calibration Reference-Only Tag
Calibration Report
Calibration Seal Tag
Certificate of Compliance-1 (for product release provision) if applicable
Certificate of Compliance-2
Certificate of Test-1 (for product release provision if applicable)
Certificate of Test-2
Conformance Checklist (included in kit - up-to-date with AS9120A)
Contract Review
Corrective Action Request
Customer Satisfaction Rating, Grand Average Spreadsheet
Customer Satisfaction Rating, Individual Customer Spreadsheet
Customer Satisfaction Survey
Data List - Parts List (if applicable)
Document Number Log
Document Revision Log
Engineering Order (for recording changes to configuration controlled documents)
First Article Inspection, General Purpose Form
First Piece Inspection (for verification and validation)
Good Material Tag (for product release if applicable)
Good Material Dot, Peel-and-Stick
Good Material Tag, Dock-to-Stock
Inspection Instruction Template
Inspection Record
Inspection Report
Inspection Summary-1
Inspection Summary-2
Inspector Stamp Log
Internal Audit Report Template
Internal Audit Schedule Spreadsheet Form
Management Meeting Report
Nonconformance Report (for control of nonconforming product)
Packing Slip/CofC (for product release if applicable)
Procedure Template-1 (for product tests if applicable)
Procedure Template-2
Product Release Record-1
Product Release Record-2
Production Inspection Record Form-1 (if applicable)
Production Inspection Record Form-2 (if applicable)
Property Certificate from Supplier
Property Control Tag
Property Management Log
Property Record
QC Tags-1 (for product release if applicable)
QC Tags-2
QC Tags-3
QMS Procedure Template
Receiving Hold Dot, Peel-and-Stick
Receiving Inspection Record
Request for Support (alternate form to control nonconforming product)
Returned Goods Disposition (for control of nonconforming product)
RFW-RFD, Commercial (request for waiver-deviation)
RFW-RFD, Mil-Spec
Shelf Life Expiration Log (if applicable)
Supplier Evaluation
Supplier Performance Rating
Supplier Performance Rating Spreadsheet
Supplier Quality Requirements
Supplier Rating Cover Letter
Supplier Survey
Training Certificate-1
Training Certificate-2
Training Log
Training Orientation Request
Verification and Validation Record (if applicable)
Warranty Product Review Report (for control of nonconforming product)
Withhold Tag
Work Instruction-1
Work Instruction-2
Work Instruction-3
Work Instruction-4VALUE ADDED WORK INSTRUCTIONS AND FORMS
Action Plan
Certificate of Material-1
Certificate of Material-2
Certificate of Origin-1
Certificate of Origin-2
Changes to ISO 9001:2000
Configuration Audit
Daily Receiving Log
Dimensional Analysis Form-1
Dimensional Analysis Form-2
Dimensional Analysis Form-3
Electro-Static Discharge Control
Impact Analysis
Information Request
Invoice - Packing Slip - CofC - Spreadsheet
Job Sheet - Work Order
Metrics
MSDS
Nonconformance Trend Chart
Process Orientation Checklist
Purchase Order
Purchase Requisition
QMS System Overview (brief overview to provide to your Customers - revise to match your business operation)
Receiving Log
Request for Quote
Requisition for Stock Control Item(s)
Routing Ticket-1
Routing Ticket-2
Routing Ticket-3
Routing Ticket-4
Shipping Log
Shipping On-Time Delivery Rating-1, Grand Average Pareto Chart
Shipping On-Time Delivery Rating-2, Individual Item ChartComplete AS9120A Kit to implement the Aviation, Space and Defense Distributor Standard, $397 (formerly Stockist Distributor)
Add to cart - instant download | View CartIf you desire to register your QMS you will need to purchase the SAE sponsored document to support your project - please visit the SAE website to purchase the AS9120A and AS9121 standards:
http://www.sae.org/technical/standards/AS9120A
http://www.sae.org/technical/standards/AS9121At-PQC™ is an "open-book" website; that is, our demo documents are WYSIWYG, which means you never take a chance with our products. What you see in our PDF evaluation documents is precisely what you receive in editable MS Word format. This guarantees you will make a well-informed decision about the documents you select for your 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.
Do you need to convert your effective QMS into an efficient quality program management system?
- Efficient QMS™ -
eQMS software transforms any quality plan to a state-of-the-art quality control program that enables your existing employees to achieve compliance to any commercial or industry sponsored quality system standard. eQMS is an efficient quality program that is operated on the world-wide-web or your company's private network to reduce overhead expenses, simplify the business operation and/or achieve a QMS pedigree - or operate with software-based project management tools.
User-friendly point-and-click operation.
Efficient QMS™ quality system software was developed to eliminate undesirable overhead expenses and labor-intensive QMS system maintenance. If you're a small business with few employees that must compete with large businesses that have a certified quality system, please click here to learn more about the Efficient QMS™ software quality management system.
A QMS pedigree requires extensive resources and tools to achieve certification, and significant overhead to maintain the system for annual assessment. eQMS was designed to achieve QMS certification using existing employees to significantly cut and eliminate overhead expenses. Most business managers set a goal to increase revenues with a QMS pedigree but call upon their employees to implement and maintain a complex QMS standard with few tools to accomplish the task - like an unfunded mandate. All our Customers consider eQMS a formidable tool in their arsenal of business resources to facilitate Company policy and keep "things" under control.
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 so much more - the 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 certification audit and helped us maintain our QMS after being downsized. The Auditors from NSF-ISR remarked that our quality program was in their top ten list of best practices."Efficient QMS(tm) 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 systems using Efficient QMS™. 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 preserving the sanity of the quality manager, which always makes it easier on the Company - then we:
built-in a daily planner with reminder capability for everybody that can't remember everything they need to do,
enabled flexibility to add or remove categories for ERP capability,
enabled on-line editing and configuration management of all procedures and work instructions using Process Maker,
enabled transition to a paperless-process by converting almost any paper form to a database-process using Form Maker,
made it easy to navigate for all Users (its a web-based interface) - and we,
know we can't mention every feature - there are too many...We invented Efficient QMS™ out of self-preservation and it has saved countless hours of labor and significantly improved the bottom-line. User's intuitively navigate eQMS because it is browser-based and because it is so convenient to access QMS documents and forms after login. We recommend installation of eQMS on an external webhost to enable "road warriors" to access project records in realtime.
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 is in no small part thanks to eQMS."
Avionics Mounts Inc.
axept Custom Engineering (MEMS)
Dynamic Paint Solutions
Dynamic Power LLC
Global Parts Inc.
K-TECHnologies Inc.
Ligi Tool and Engineering Inc.
McAllister Tool and Machine
Nee's Machine Inc.
Nomad Aviation Inc. Testimonial: "We passed our ISO 9001:2008 registration audit thanks to Efficient QMS...Thank you."
Sandia National Laboratories
Specialty Metals Corporation
Sustainable Energy Technologies
Theranos
Price: $697 includes ISO 9001 or AS9100C, AS9110A, AS9120A or AISC (other QMS systems available with prior notice).
Add to Cart | View Cart (delivery via email)
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 program 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 program or voluntary quality management system!
How will your business spell relief?
Efficient QMS™
Quality Plan
Purpose of the Quality Plan
The quality plan is the document setting out the quality assurance procedures for the project. Its aim is to assure that the results and deliverables of the project are of high quality and meet the specifications set in the project description of work. Once accepted, the quality plan becomes an official project document, which should govern all actions of the business operation.
Scope of the Quality Plan
The quality plan is to be used by:
all parties responsible for preparing and amending deliverables,
quality experts responsible for reviewing completed quality plans and sign-off,
any responsible person of the business operation that is charged with approving work to be done by third parties to enable completion of deliverables.
Procedure Description
Quality planning is an integral part of management planning. As a pre-requisite to its preparation, the quality assurance manager must review all requirements to determine the necessary activities that need to be planned. The quality plan must be prepared early in the project to demonstrate and provide the business operation with the assurance that:
the contract requirements and conditions have been reviewed,
effective quality planning has taken place,
the quality system is appropriate.
To ensure relevance of the quality plan, the quality assurance manager should conduct quality reviews throughout the duration of the contract and when contractual changes occur. The quality assurance manager must ensure that the quality plan is available to all concerned and that its requirements are met.
Quality within a Project
Activities must be implemented, including their sequence, to ensure that the project and its deliverables conform to the project requirements. Personnel responsible for ensuring that the required activities are carried out should be identified within the document. The quality plan should include explanations that are necessary to show how quality requirements for activities are met. A list of such activities should include:
responsibilities of the quality assurance manager,
quality system review,
document and data control,
project quality control board,
internal communication strategies,
prototype identification and traceability,
inspection and testing of project prototypes and their parts,
peer review and control of non-conforming deliverables,
corrective and preventive actions.
Deliverable Documents
Official project documents should be produced in standard format with standard font size, page layout with headers and footers and standard justification. Deliverables should:
have a list of abbreviations used within the deliverable
have a table of contents
have a list of figures
have a list of tables
start with a one-page executive summary
end the main part with a conclusions section
include a references section after the conclusions section
include all detailed technical and other information in appendices
language should be English
display the same fonts throughout the document
be spell-checked
Compatibility Guaranteed!
If you cannot edit At-PQC™ document(s) in your MS Word or Excel program we will fix it or refund your purchase.
Can't find what you're looking for...?
Email At-PQC™:
At-PQC™
JnF Specialties, LLC
664 Greenscape Lane
Colorado Springs, Colorado
Cell Phone Support: (719) 649-4242 [6:00am to 6:00pm MT 7-days-a-week]
Fax: (719) 573-4205
Visit with At-PQC™ about any aspect of your improvement project during your office hours.
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Send an email to request next-day support or call our helpline during your office hours.
We're here to support your quality assurance project with our full attention and we know our website and experience will enable you to quickly and efficiently complete your quality assurance project to proceed with the next action item on your list.
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