SBS - The Best Value in QMS software

C4i - Control, Capability, Compliance and Continuous Improvement?

Elsmar Forum Sponsor

E Wall

Just Me!
Super Moderator
#2
Nope

Sorry...cannot recall anyting.

I tried a search on the web but only came up with information associated with C4I and Navy site which clearly has nothing to do with continuous improvment of quality systems.

Eileen
 

Randy

Super Moderator
#3
Yep....have about 29 years years with C3I stuff. The computer stuff involves intigration of all the elements electronically.

Why?:confused:
 

gpainter

Quite Involved in Discussions
#4
Thought it might be a spinoff of a military initiative and now a Quality initiative??? Still seraching for info, will post if I find any.
 

gpainter

Quite Involved in Discussions
#5
Came across this C4I = Control, Capability, Compliance and Continuous Improvement. But no other info as to if this is a new program/initiative by someone to make money to help Quality. Keep Searchi'n
 

Marc

Fully vaccinated are you?
Staff member
Admin
#6
gpainter said:
Has anyone any knowledge of something called C4I in association Continuous Improvement?
I was looking through some old threads and came upon this one.

gpainter - Where did you come across C4I?

All the searches I did gave me "Command, Control, Communication, Computer, Intelligence". Anyone have any other info?
 

gpainter

Quite Involved in Discussions
#7
It has been awhile, but I believe it was something that Whirlpool is doing. Not 100% sure. Not sure of the sight that I found C4I at.
 
Last edited:
A

Atul Khandekar

#8
Marc said:
All the searches I did gave me "Command, Control, Communication, Computer, Intelligence". Anyone have any other info?
I remember having tried a web search but came up with the same thing. The only fleeting reference I found was on Tom Pearson's site at http://www.reciprocalonline.com/dev/index.asp

"C" the difference in your business...
Some organizaitons talk about Control, Capability, Compliance, and Continuous Improvement (C4I). However, it is important to remember that there are levels of performance in each of these areas that define how an organizaiton will compete in its market. The overall rate at which an organization improves relative to its competition (their Capability Improvement Ratio) is critical to long term success.
 

gpainter

Quite Involved in Discussions
#9
Atul is correct and that is where I saw it also. I now have seen the mention of C3I = Command, Control, Communications and Information. Just wanted more info,if anyone had first hand knowledge. Tom Pearson is a consultant working for Reciprocal and also has co-written a six sigma book "Wi$dom on the Green (Smarter Six Sigma Solutions).
 
Thread starter Similar threads Forum Replies Date
R Control Methods in Control Plan FMEA and Control Plans 0
M Design Control - Management of Electronic CAD files Design and Development of Products and Processes 11
S TSCA (Toxic Substances Control Act) PIP 3:1 RoHS, REACH, ELV, IMDS and Restricted Substances 0
S Use of Attributes Control Charts Statistical Analysis Tools, Techniques and SPC 1
U Appraiser Out of Control Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 5
L Looking for Control Plan and FMEA Stamping process FMEA and Control Plans 2
Z AS9100 Control of Nonconforming Outputs - Rework Dispositions AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
K ASME, ANSI, ASTM and similar specifications and their requirements for document control. Inspection, Prints (Drawings), Testing, Sampling and Related Topics 8
Z Software for design control ISO 13485:2016 - Medical Device Quality Management Systems 3
K Quality Control/Assurance in the Metal Industry Quality Tools, Improvement and Analysis 10
K Defining risk control measures IEC 62304 - Medical Device Software Life Cycle Processes 14
J Warehouse temperature and humidity control EU Medical Device Regulations 7
Jimmy123 IATF16949 Control Plan FMEA and Control Plans 1
D Control Number for Class III and IV devices Canada Medical Device Regulations 1
J Document Control Metrics Document Control Systems, Procedures, Forms and Templates 3
I Document Control Software Document Control Systems, Procedures, Forms and Templates 2
T Controlling Expandable Forms in Paper-Based Document Control System Document Control Systems, Procedures, Forms and Templates 10
N ISO 13485 7.3.9 Change control in medical device software ISO 13485:2016 - Medical Device Quality Management Systems 6
C UDI Questions on Control Units Other US Medical Device Regulations 6
A Quality Control Datasheets Inspection, Prints (Drawings), Testing, Sampling and Related Topics 2
M Control-self assessment Internal Auditing 5
GreatNate Master Control QMS software Quality Tools, Improvement and Analysis 0
A Prototype control plan FMEA and Control Plans 2
J Records Control - Does each individual record need to be numbered? Records and Data - Quality, Legal and Other Evidence 2
shimonv Document Control Procedure Header Content Document Control Systems, Procedures, Forms and Templates 3
W FMEA - Current control and occurrence rating FMEA and Control Plans 3
S Which department should prepare the control plan? could you show me a standard regarding to this matter. FMEA and Control Plans 17
G Control Plan & PFMEA Review Procedure? FMEA and Control Plans 8
N What are the software audit and control steps Reliability Analysis - Predictions, Testing and Standards 2
A Fabric roll inspection - What type of Control Chart to use? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 2
C Monitoring and Control Instruments RoHS, REACH, ELV, IMDS and Restricted Substances 3
M ISO14971:2019 - Verification of implementation and effectiveness of risk control ISO 14971 - Medical Device Risk Management 3
T Risks arising from control measures vs. ineffective control measures ISO 14971 - Medical Device Risk Management 11
J Need Change Control Yes/No Decision Tree Template ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
P IQ, OQ, PQ protocol, and report templates for Distributed Control Systems in Pharmaceutical Manufacturing Systems. Qualification and Validation (including 21 CFR Part 11) 0
R Risk control measures as per ISO 14971 ISO 14971 - Medical Device Risk Management 6
T Linking Control Plans and PFMEA's FMEA and Control Plans 3
L How to add exemption or statement to control of document procedure? ISO 13485:2016 - Medical Device Quality Management Systems 5
T PFMEA and Control Plans on legacy product FMEA and Control Plans 5
P IATF 16949 requirement - error-proofing in control plan IATF 16949 - Automotive Quality Systems Standard 3
C 8.5.1.1 Control of Equipment, Tools, and Software Programs - Questions about the extent of control of NC programs AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
Q Version/Revision Control of CAD files Document Control Systems, Procedures, Forms and Templates 2
earl62 What is the best way to control special characteristics in Control plan? Is it Mandatory to have SPC for IATF 16949? IATF 16949 - Automotive Quality Systems Standard 12
I Control Plan (Product/Process specification/ Tolerance) acceptance FMEA and Control Plans 27
Sravan Manchikanti How to interpret '8.3 Control of nonconforming product' for SaMD device while implementing ISO 13485 & MDSAP ISO 13485:2016 - Medical Device Quality Management Systems 7
Z Putting back excluded rows/data points in a control chart Using Minitab Software 0
J Control Plan use on the manufacturing floor FMEA and Control Plans 4
E Change in control plan - Do I have to do sampling? IATF 16949 - Automotive Quality Systems Standard 1
D All Dimensions listed on control plan FMEA and Control Plans 10
W Need for current design or process control FMEA and Control Plans 2

Similar threads

Top Bottom