Control of NCM: segregation strategies

sulkinsf

Involved In Discussions
#1
I am looking for generally accepted rules for segregating product.

For example,

1) A designated Nonconformance hold area on the floor, needs clearly painted boarders and red fill/black font, 5"x9" sign on wall or post.

2) Nonconformance Shelf needs red, 1" label.

I would like to hear what rules are being applied out in the field to segregate.

Thanks,

Steve.
 
Elsmar Forum Sponsor

barb butrym

Quite Involved in Discussions
#2
anything goes...actually.

tags, bags, bins, shelfs, totes, shrink wrap, locked cages...my personal favorite for big stuff is movable posts connected with plastic chain link (color coded of course...LOL) much as you would see for bank lines and such...just set it up around it, skid and all.

Rule is simple "keep it from getting mixed"....thats really what its all about...protect the good stuff.
 
Thread starter Similar threads Forum Replies Date
N Nonconforming Material (NCM) Control in very Small Manufacturing Companies ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
Q ISO 9001 8.5.1 - Control of production and service performance ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
A What is the difference between Design Process, Process Design and Design Control? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
A Beginners help with ISO3951-2 Combined control s-method n>5 what is Phi ?? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 0
C Corrective action for failure in documents control ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
B Control chart and sample time Statistical Analysis Tools, Techniques and SPC 1
DuncanGibbons Manufacturing Plan vs Material Specification vs Control Plan Manufacturing and Related Processes 4
J Control chart for huge sample size Statistical Analysis Tools, Techniques and SPC 9
K Contamination Control - Class Is medical devices (Clause 6.4.2 ISO 13485:2016 (E)) ISO 13485:2016 - Medical Device Quality Management Systems 11
J 510(k) for a control kit for an external IVD test kit 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
T Assessing Hazard-Related Use Scenarios where control measures exist through standards IEC 62366 - Medical Device Usability Engineering 14
adir88 Documenting Risk Control Option Analysis ISO 14971 - Medical Device Risk Management 8
T Design Control Procedures later in the Development Process ISO 13485:2016 - Medical Device Quality Management Systems 6
L AS5553 Clause 3.1.7 e "Control packaging material ..................reused" AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 0
T Attributes SPC study - Attributive control (Go gage) Statistical Analysis Tools, Techniques and SPC 5
K Process Mapping - Inputs/Outputs/Detail Activities/Control points/Measurement? Process Maps, Process Mapping and Turtle Diagrams 4
S Should safety checks be included in the Control Plan? IATF 16949 - Automotive Quality Systems Standard 5
D Infrastructure: Equipment, Work Environment and Contamination Control ISO 13485:2016 - Medical Device Quality Management Systems 4
Q Relabeler for patent expired product - design control responsibilities? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
J How to make Quality Control plans Quality Tools, Improvement and Analysis 5
I Document Control on Log Files ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
Q Tracking Procedure Revisions (Document Control) Document Control Systems, Procedures, Forms and Templates 9
C Document Control Stamps - Does anyone still stamp their documents? Document Control Systems, Procedures, Forms and Templates 21
D Supplied Product on Control Plan - Lot ranging in 40,000 pcs per product FMEA and Control Plans 3
D IEC 62304 Risk Classification - With and without hardware control IEC 62304 - Medical Device Software Life Cycle Processes 2
J Antiviral Mask or Mask to Mitigate or Control Corona Virus Manufacturing and Related Processes 22
A UDI and Design Controls - Labeling change via the Design Control process 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
I Control of Documentation Distribution - Document Control ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
S Inventory Control - Any thoughts would be appreciated ISO 13485:2016 - Medical Device Quality Management Systems 2
H SPC for special characteristics - CSR - Control of SC and CC Statistical Analysis Tools, Techniques and SPC 1
T Control of downloaded document copies by employees Document Control Systems, Procedures, Forms and Templates 3
T Document control ISO 13485:2016 ISO 13485:2016 - Medical Device Quality Management Systems 5
M Is there any pre-defined Control plan format/template acc. VDA? VDA Standards - Germany's Automotive Standards 0
B Record Management - Does the QMS need to control templates of records? Records and Data - Quality, Legal and Other Evidence 17
O Inventory control ideas - I have an open stock room with a "sign out" book Manufacturing and Related Processes 9
V IATF 16949 8.4.1 Control of externally provided processes, products and services - Should the CB be on our Approved Supplier List? IATF 16949 - Automotive Quality Systems Standard 10
R Process control documents - Context of API Spec Q1, Clause 5.7.1.3 Other ISO and International Standards and European Regulations 0
D Performance specification as a Risk Control Measure, EN 14971 ISO 14971 - Medical Device Risk Management 7
L Form-dependent position prevention control FMEA and Control Plans 1
S CQI-23 - Molding System Assessment - Control of part weight IATF 16949 - Automotive Quality Systems Standard 5
D Change Control - Product Name Change and its associated labeling EU Medical Device Regulations 7
S Degree of control of distributors - PMS EU Medical Device Regulations 2
M What is "setup control chart"? Statistical Analysis Tools, Techniques and SPC 2
Jimmy123 What is the difference between Error Proofing and Controls? ISO/IATF 16949 - Control Plans FMEA and Control Plans 16
V IS/ISO/IEC 17025:2017 Clause 7, sub clause 7.11 Control of data and information management ISO 17025 related Discussions 1
C Design Control - Ways of capturing inputs from manufacturing Other Medical Device Related Standards 5
G Control Plan - Include the processes for each sub component? APQP and PPAP 2
U Change Management vs Change Control? Design and Development of Products and Processes 4
F Control of medical device IFU content Other Medical Device and Orthopedic Related Topics 3
Jimmy123 FMEA - Preventive vs Detection Control FMEA and Control Plans 7
Similar threads


















































Top Bottom