7.2.2 Review of Requirements Related to the Product

H

Hooman

#1
Review of requirements related to the product

Could you please explain for me the note in the clause7-2-2?

" In some situations, such as internet sales, a formal review is impractical for each order. Instead the review can cover relevant product information such as catalogues or advertizing material. "
 
Elsmar Forum Sponsor
E

energy

#2
Seld explanatory?

To me, and I'm using it in my Quality Plan, it means that a Customer can order a catalog item over the Internet or in reponse to a sales Flyer and you don't all have to sit down in a huddle and decides what the Customer wants. The old "Contract Review" element. Maybe I'm wrong, but I'll argue it when the time comes. JMHO Welcome to the Cove!:bigwave: :ko: :smokin:
 

JodiB

Still plugging along
#3
Agreed

The onus of "contract review" falls to your advertising or marketing department to make sure that the information in your catalog is accurate : part number, description, price, etc. This is the offer of your product.

Then the customer relies on this description of product to place his order, which becomes his acceptance of your offer. A contract has been made.

No further review is necessary. It is assumed that the information provided by your company is accurate and the customer is fully informed.
 
#4
Contract review

energy and Lucinda have it pretty much right. You must remember that this ISO thing could apply to any business. Way back in the days of catalog sales, the purchaser would either fill out an order form and mail it in or call a phone number to place the order. Contract review in those cases was nothing more than making sure the customer gave all the information needed to fill the order. In some cases I have been notified that my order could not be filled at that time and I had a choice to cancel the order or wait for the ‘backorder’ to be filled. Hey! 7.2.1 b) in action! :rolleyes:
 
Thread starter Similar threads Forum Replies Date
G Review of Requirements related to the Product (7.2.2) ISO 13485:2016 - Medical Device Quality Management Systems 1
A Review of requirements related to the product - 7.2.2 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 14
E AS9100 7.2.2 Review of Requirements Related to the Product AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
M 7.2.2 Review of Requirements Related to the Product (Design-Manufacturing Service) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
F Review of Requirements Related to the Product - Clause 7.2.2 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
G Management Review 5.6.3 b) Improvement of product related to customer requirements Management Review Meetings and related Processes 7
S ISO 9001 Clause 8.2.3 - Review of the requirements for products and services in a Cafe ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
D Engineering Drawing Review and Approval Requirements ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
S List of requirements for Management Review in IATF 16949 IATF 16949 - Automotive Quality Systems Standard 9
J ISO 9001:2015 8.2.3 - Review of Requirements (Clarification on compliance) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
B IATF 16949 Cl. 8.2.3.1.1 - Review of the Requirements for Products and Services IATF 16949 - Automotive Quality Systems Standard 15
T Inspection Form Review And Approval - FDA Requirements ISO 13485:2016 - Medical Device Quality Management Systems 2
T Document Review And Sign Off Second Person Review - FDA Requirements ISO 13485:2016 - Medical Device Quality Management Systems 5
L IVD Reagent Techncial File Review Requirements (IVDD Annex III) EU Medical Device Regulations 4
W Evidence for Review of Requirements - AS9100 Clause 7.2.2 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
G ISO 14001 & Product Design Process Environmental Aspect Review Requirements ISO 14001:2015 Specific Discussions 7
H Form that will satisfy Design Review and Design Verification Requirements (7.3) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
J Requirements for Review and Approval of QMS Documents Document Control Systems, Procedures, Forms and Templates 14
J FDA Annual Product Review (APR) Requirements US Food and Drug Administration (FDA) 1
M 21 CFR Part 210-211 Sec. 211.192 Production Record Review Requirements Document Control Systems, Procedures, Forms and Templates 5
M 7.6.3.1 Requirements for Capability to Perform Tests Correctly - Review of Records IATF 16949 - Automotive Quality Systems Standard 10
V Document Review Requirements for SQF 2000 (Safe Quality Food Standard) Various Other Specifications, Standards, and related Requirements 3
S TS 16949 Requirements for Timely Review of Engineering Specifications IATF 16949 - Automotive Quality Systems Standard 6
F Periodic Review Requirements for Software - Medical DeviceS Software Quality Assurance 2
U Medical Device Design Review Records Requirements Design and Development of Products and Processes 16
R FDA CDRH Premarket Review Requirements - Submission Cover Sheet 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
L ISO 9001 Document Review and Approval Form Requirements Document Control Systems, Procedures, Forms and Templates 6
T Fulfilling ISO 9001 Document Review Requirements Document Control Systems, Procedures, Forms and Templates 21
M AS9100 7.2.2 Review of Requirements - Order & Product Review Records AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
G Audit Nonconformance - 7.2.2 - Contract Review (Review of Requirements) Contract Review Process 16
B Differentiating between "Review of Requirements" and "Contract Review" AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
T Periodic Quality Manual and Procedure Review Requirements General Auditing Discussions 5
S TS 16949 Clause 5.6 - Management Review Requirements - Without a meeting? IATF 16949 - Automotive Quality Systems Standard 17
M Management Review Input and Output Content Requirements Quality Management System (QMS) Manuals 2
J Supplier Purchase Order Review and Approval Requirements IATF 16949 - Automotive Quality Systems Standard 3
O Management Review Inputs and Outputs - AS9100 Registration Audit Requirements Management Review Meetings and related Processes 16
C AS9100 7.2.2 Review of requirements AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 7
C Review and Implementation of Customer Requirements ISO 13485:2016 - Medical Device Quality Management Systems 6
J Purchase Order Review to meet the requirements of clause 7.4.2 in a small company ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
M TS16949-Requirements of 5.6 Management Review Management Review Meetings and related Processes 3
R Medical Device Product Requirements Document (PRD) a "Design Review"? Design and Development of Products and Processes 4
U Management Review requirements - ISO 9001 Clause 5.6 and URAC requirements Management Review Meetings and related Processes 7
J IVD Directive - Review and Update Essential Requirements Documentation EU Medical Device Regulations 5
T Feasibility Review - How are you meeting 7.2.2 and 7.2.2.2 requirements? IATF 16949 - Automotive Quality Systems Standard 18
Q Management Review Requirements - TS 16949 Clause 5.6.1 Management Review Meetings and related Processes 17
T Management Review and Audit Data Requirements Management Review Meetings and related Processes 11
A At what stage do you review new product statutory / regulatory requirements? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
T Feasibility review prior to quoting - Requirements Review - 7.2.2 Feasibility Help ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
Q PPT used as Design Review ISO 13485:2016 - Medical Device Quality Management Systems 3
bryan willemot Contract Review and risk managment AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2

Similar threads

Top Bottom