SBS - The best value in QMS software

Contract / Customer Order Review Checklist Needed

Nicole Desouza

Nicole Desouza

Involved In Discussions
#11
#11
Golfman25 said:
Why do a checklist. Just review the order, initial and date.
Click to expand...
Because we need something to help us not to forget very important details. The easiest way that I know how to do that is to implement a checklist that lists all of the items we have mistakenly overlooked over the past 3 months (since I have been working here) during the contract review / customer order review process.
 
Elsmar Forum Sponsor
A

Al Rosen

Staff member
Super Moderator
#13
#13
Nicole Desouza said:
Because we need something to help us not to forget very important details. The easiest way that I know how to do that is to implement a checklist that lists all of the items we have mistakenly overlooked over the past 3 months (since I have been working here) during the contract review / customer order review process.
Click to expand...
Start with the items that were overlooked in the last 3 months.
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
B How to Conduct a Review of Customer Order (Contract Review)? Contract Review Process 5
B Interesting Discussion The legal aspects of Customer Specific Requirements (Contract Law). IATF 16949 - Automotive Quality Systems Standard 12
I Implant Raw Material Supplied from Customer to Contract Manufacturer ISO 13485:2016 - Medical Device Quality Management Systems 1
R Customer Feedback - ISO 13485 Section 8.2.1 - Small Contract Manufacturer ISO 13485:2016 - Medical Device Quality Management Systems 9
W Supporting the Customer after Termination of a Contract Other Medical Device and Orthopedic Related Topics 2
M Tainted wipes maker Triad sues contract manufacturing customer 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
R 7.2.1 Customer Requirements Checklist for a Small Contract Manufacturing Machine Shop AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
R Document Control: Contract between my company and customer Document Control Systems, Procedures, Forms and Templates 4
E Customer Satisfaction - Customer Perception of Government Contract Officers ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
G Inspection by Attributes to ensure a 99% Confidence in a Customer Contract Inspection, Prints (Drawings), Testing, Sampling and Related Topics 6
T Electronic Industry Contract Manufacturing - Customer notification needed? Supplier Quality Assurance and other Supplier Issues 1
Q Question about Circumstances - Customer Prints and Changes after Contract Acceptance Misc. Quality Assurance and Business Systems Related Topics 12
B Does FDA Registration QSR need to cover non-medical devices for contract repackager? US Food and Drug Administration (FDA) 1
J Need a contract monitoring Tool General Information Resources 0
Y Procedures on Contract Review Document Control Systems, Procedures, Forms and Templates 3
C SharePoint Contract Management Software General Information Resources 0
A Medical Device Contract Manufacturer - Does the CM need to register with FDA? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
M How Specific in an ISO 13485:2016 Scope for a Contract Manufacturer ISO 13485:2016 - Medical Device Quality Management Systems 9
T Selection Of Contract Manufacturers Supplier Quality Assurance and other Supplier Issues 2
chris1price Contract Sterilization Service Providers ISO 13485:2016 - Medical Device Quality Management Systems 5
A Requirements for Contract Manufacturers Other Medical Device and Orthopedic Related Topics 3
H Obligations as a contract manufacturer during an MDSAP audit ISO 13485:2016 - Medical Device Quality Management Systems 5
Nikki9154 MDSAP inquiry for China Contract Manufacturers ISO 13485:2016 - Medical Device Quality Management Systems 4
H 510k with Contract Manufacturer Other US Medical Device Regulations 2
bryan willemot Contract Review and risk managment AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
J Can signed agreements over-ride review of every "contract" under ISO 13485:2016? ISO 13485:2016 - Medical Device Quality Management Systems 2
JoCam FDA Registration for Sub-contract manufacturers Medical Device and FDA Regulations and Standards News 2
E Contract manufacturer FDA requirements foreign company US Food and Drug Administration (FDA) 6
M We are looking for a Contract Manufacturer US Food and Drug Administration (FDA) 2
L Sample Procedure from Contract Manufacturer Prospective ISO 14971 - Medical Device Risk Management 1
I Is the contract mfg. mentioned in legal manufacturer EC certificate? CE Marking (Conformité Européene) / CB Scheme 4
S Can a Contract Manufacturer "release" product on behalf of client to the market? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
R FCC certification (contract manufacturer) TL 9000 Telecommunications Standard and QuEST 1
C Contract Review with Multiple Line items ISO 13485:2016 - Medical Device Quality Management Systems 7
K ANVISA B-GMP Auditing requirements for Contract Manufacturers Other Medical Device Regulations World-Wide 1
M Contract manufacturer MDR Quality Management System (QMS) Manuals 1
A Medical Device Contract Manufacturing Requirements and Information - Help wanted ISO 13485:2016 - Medical Device Quality Management Systems 5
G Is ISO 9001:2015 certification worth it for a company that does only contract manufacturing? Quality Management System (QMS) Manuals 14
K Reporting a Change of Contract Manufacturer for a 510(k) cleared device Other US Medical Device Regulations 5
A What if Contract Manufacturers does not have an ISO 13485 certificate? Where will the NB audit take place, at legal mfg. site or contract mfg. site? Other Medical Device Regulations World-Wide 3
O Identifying KPI for AS9100 8.1.4 - Prevention of Counterfeit Parts - PCB assembly contract manufacturer AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 16
M Contract Manufacturers and MDF Responsibilities, ISO 13485:2016, Clause 4.2.3 ISO 13485:2016 - Medical Device Quality Management Systems 3
M Medical Device Master File - We are a contract manufacturer ISO 13485:2016 - Medical Device Quality Management Systems 7
D Software Validation - Contract manufacturer of Components (PCBA's) Qualification and Validation (including 21 CFR Part 11) 7
Ed Panek Moving from Contract Manufacturing to Production In-House ISO 13485:2016 - Medical Device Quality Management Systems 3
J Contract Sterilization - Our company is a contract manufacturer Manufacturing and Related Processes 8
R Contract Manufacturer/OEM Supplier - We are a specification developer for a kitted product 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
S Legal Manufacturer FDA Reporting Obligations for Using New Contract Sterilization Site Other Medical Device Regulations World-Wide 0
L REACH Compliance - Small, family-owned contract manufacturer REACH and RoHS Conversations 16
R 21 CFR Part 820 Contract Manufacturer of Medical Device Component 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4

Similar threads

Top Bottom