Menu
Forums
New posts
Search forums
What's new
New posts
All posts
New media
New media comments
Latest activity
Media
New media
New comments
Search media
Resources
Latest reviews
New resources
Search resources
Attachment List
Log in
Register
What's new
Search
Search
Everywhere
Discussion Threads
This forum
This thread
Search titles only
By:
New posts
Search forums
Menu
Log in
Register
Forums
Common Quality Assurance Processes and Tools
FMEA and Control Plans
JavaScript is disabled. For a better experience, please enable JavaScript in your browser before proceeding.
How to define the measurement technique and control method for manual soldering
Thread starter
TYCOALAN
Start date
May 18, 2010
Prev
1
2
First
Prev
2 of 2
Go to page
Go
T
TYCOALAN
May 24, 2010
#11
May 24, 2010
#11
thank you all for the input.
Elsmar Forum Sponsor
Prev
1
2
First
Prev
2 of 2
Go to page
Go
You must log in or register to reply here.
Thread starter
Similar threads
Forum
Replies
Date
S
How to define Permissible Error for Measurement and Test Equipment?
Measurement Uncertainty (MU)
3
Apr 13, 2011
A
Define timeline for Major and Miner Audit finding
General Auditing Discussions
4
Apr 5, 2021
T
How do you define your Hazards? <a Risk Management discussion>
ISO 14971 - Medical Device Risk Management
16
Apr 9, 2020
M
Define voltage and frequency to perform tests 61010-1 and 61326-1 for CE certification
CE Marking (Conformité Européene) / CB Scheme
4
Nov 20, 2019
I
Sampling processes - Who must define the AQL level?
AQL - Acceptable Quality Level
9
Jun 14, 2019
V
Who should define and own the Design and Development Plan and how to maintain the updates and revisions.
ISO 13485:2016 - Medical Device Quality Management Systems
2
May 26, 2019
S
API Spec Q1 - How to define Management Representative competency for QMS
Oil and Gas Industry Standards and Regulations
12
Apr 11, 2019
M
How To Define ISMS (information Security Management System) Scope
IEC 27001 - Information Security Management Systems (ISMS)
18
Mar 13, 2019
K
How to define Expected life service life of medical device
Other Medical Device Related Standards
4
Mar 5, 2019
S
How to Define Importers under EU MDR / Brexit
EU Medical Device Regulations
3
Oct 18, 2018
M
Should Potential Customer Complaint Outcome Define Registrar NC Rating?
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
8
Dec 11, 2017
K
ISO 9001:2015 clause 9.2.2 a. - Define the audit criteria and scope
Internal Auditing
2
Oct 31, 2017
Q
QI Macro Histogram - Can someone define *sorted data*?
Capability, Accuracy and Stability - Processes, Machines, etc.
7
Sep 15, 2017
H
How to define Root Cause when some points are out of control chart
Statistical Analysis Tools, Techniques and SPC
6
Sep 6, 2017
I
How do you define Risk (Medical Device)?
ISO 14971 - Medical Device Risk Management
30
Apr 21, 2017
M
SOP or template for a study to Define Storage Conditions of Orthopaedic Implants
EU Medical Device Regulations
3
Mar 29, 2017
D
Definition
Client - How does the government define their clients?
Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically
1
Mar 26, 2017
How to define a Risk Based Approach for Supplier Management per ISO 13485:2016
ISO 13485:2016 - Medical Device Quality Management Systems
1
Jan 29, 2017
G
How to define the scope of QMS as per ISO 9001:2015
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
21
Sep 1, 2016
R
How to define QMS certification scope statement?
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
11
Jun 24, 2015
R
Review of "Key Data" for contract labs, but SOP doesn't define "key data". Problem?
Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations)
2
May 7, 2015
G
Procedure to define Signing Authority for Procurement Limits
ISO 13485:2016 - Medical Device Quality Management Systems
2
Apr 13, 2015
P
Can a company define new quality standards for special industry
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
2
Jan 13, 2015
L
Are there any requirements to define barcode requirements ?
Misc. Quality Assurance and Business Systems Related Topics
2
Oct 23, 2014
X
How to define Calibration Acceptance Criteria
General Measurement Device and Calibration Topics
3
Oct 7, 2014
H
ISO 17025 - How to define a "Test Equipment" ?
ISO 17025 related Discussions
2
Sep 3, 2014
J
Where do you define Internal Auditor qualifications?
Internal Auditing
9
Jun 9, 2014
V
Is there an approach to define the "must 'or' should" in supplier audits?
US Food and Drug Administration (FDA)
2
Apr 20, 2014
T
Internal Audit - How to define the Importance of Departments and Processes
Internal Auditing
8
Feb 5, 2014
T
Help me understand how to define Processes
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
40
Jan 21, 2014
L
How to define R & D Receiving (Incoming) Inspection Plan
Design and Development of Products and Processes
18
Dec 26, 2013
B
How to define and implement Configuration Management
Document Control Systems, Procedures, Forms and Templates
5
Mar 8, 2013
C
How to Define and Document Controls of Outsourced Processes
Food Safety - ISO 22000, HACCP (21 CFR 120)
5
Feb 7, 2013
S
Please help me define training requirements for a Career in Regulatory Affairs
21 CFR Part 820 - US FDA Quality System Regulations (QSR)
2
Nov 10, 2012
K
How to define the Acceptances Criteria for all equipment?
Manufacturing and Related Processes
7
Oct 13, 2012
L
Definition
Program - How do you define Program with regard to ISO 9001?
Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically
3
Jun 20, 2012
A
Supplier Evaluation SOP - How do I Define Major and Minor Suppliers?
Supplier Quality Assurance and other Supplier Issues
14
May 22, 2012
Q
Where to define Authorities and Responsibilities in Documentation?
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
1
Apr 2, 2012
J
Define Energy Used/Delivered - Applicable to Electrical or Mechanical Power or both?
21 CFR Part 820 - US FDA Quality System Regulations (QSR)
1
Mar 6, 2012
R
820.50 (A) (2)Define the Type and Extent of Control to be exercised over Vendor
Misc. Quality Assurance and Business Systems Related Topics
5
Feb 28, 2012
A
Where to define Process Tailoring Form used in CMMI in the ISO 9001 Quality Manual?
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
5
Feb 7, 2012
Q
Criteria to define QMS processes in ISO/TS 16949:2009
IATF 16949 - Automotive Quality Systems Standard
23
Nov 16, 2011
S
How to define New Equipment? Device is Returned, Refurbished or Repaired
Misc. Quality Assurance and Business Systems Related Topics
3
Oct 18, 2011
C
Controlling Documents: Beyond the standard, how do we truly define what to control
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
9
Sep 28, 2011
C
How to define Process Special Characteristics (SC)
FMEA and Control Plans
4
Sep 14, 2011
What is the meaning of "define/defined" in ISO 9001?
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
19
Aug 19, 2011
Local Control Document procedure....define it or not?
Document Control Systems, Procedures, Forms and Templates
24
Aug 3, 2011
M
Excel Templates for Plan & Define Phase in NPI Process for Tire Manufacturer
Excel .xls Spreadsheet Templates and Tools
1
May 13, 2011
R
Define Data from Taguchi to Response Surface Methodology in Minitab
Using Minitab Software
2
May 12, 2011
K
How to define PVC Pellet Quality
Manufacturing and Related Processes
8
Apr 26, 2011
Similar threads
S
How to define Permissible Error for Measurement and Test Equipment?
Started by senray897
Apr 13, 2011
Replies: 3
Measurement Uncertainty (MU)
A
Define timeline for Major and Miner Audit finding
Started by AADIVISH
Apr 5, 2021
Replies: 4
General Auditing Discussions
T
How do you define your Hazards? <a Risk Management discussion>
Started by ThatSinc
Apr 9, 2020
Replies: 16
ISO 14971 - Medical Device Risk Management
M
Define voltage and frequency to perform tests 61010-1 and 61326-1 for CE certification
Started by Michelrsilva
Nov 20, 2019
Replies: 4
CE Marking (Conformité Européene) / CB Scheme
I
Sampling processes - Who must define the AQL level?
Started by invitro_spain
Jun 14, 2019
Replies: 9
AQL - Acceptable Quality Level
V
Who should define and own the Design and Development Plan and how to maintain the updates and revisions.
Started by v9991
May 26, 2019
Replies: 2
ISO 13485:2016 - Medical Device Quality Management Systems
S
API Spec Q1 - How to define Management Representative competency for QMS
Started by SACHIN GUPTA
Apr 11, 2019
Replies: 12
Oil and Gas Industry Standards and Regulations
M
How To Define ISMS (information Security Management System) Scope
Started by maurice
Mar 13, 2019
Replies: 18
IEC 27001 - Information Security Management Systems (ISMS)
K
How to define Expected life service life of medical device
Started by Kuldeep Singh
Mar 5, 2019
Replies: 4
Other Medical Device Related Standards
S
How to Define Importers under EU MDR / Brexit
Started by snowball852
Oct 18, 2018
Replies: 3
EU Medical Device Regulations
M
Should Potential Customer Complaint Outcome Define Registrar NC Rating?
Started by MrPhish
Dec 11, 2017
Replies: 8
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
K
ISO 9001:2015 clause 9.2.2 a. - Define the audit criteria and scope
Started by kylerf
Oct 31, 2017
Replies: 2
Internal Auditing
Q
QI Macro Histogram - Can someone define *sorted data*?
Started by qcman
Sep 15, 2017
Replies: 7
Capability, Accuracy and Stability - Processes, Machines, etc.
H
How to define Root Cause when some points are out of control chart
Started by hiepyeuh
Sep 6, 2017
Replies: 6
Statistical Analysis Tools, Techniques and SPC
I
How do you define Risk (Medical Device)?
Started by indubioush
Apr 21, 2017
Replies: 30
ISO 14971 - Medical Device Risk Management
M
SOP or template for a study to Define Storage Conditions of Orthopaedic Implants
Started by mpfizer
Mar 29, 2017
Replies: 3
EU Medical Device Regulations
D
Definition
Client - How does the government define their clients?
Started by donaldj
Mar 26, 2017
Replies: 1
Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically
How to define a Risk Based Approach for Supplier Management per ISO 13485:2016
Started by alonFAI
Jan 29, 2017
Replies: 1
ISO 13485:2016 - Medical Device Quality Management Systems
G
How to define the scope of QMS as per ISO 9001:2015
Started by gaurav16949
Sep 1, 2016
Replies: 21
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
R
How to define QMS certification scope statement?
Started by Roody5617
Jun 24, 2015
Replies: 11
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
R
Review of "Key Data" for contract labs, but SOP doesn't define "key data". Problem?
Started by Robert in SF
May 7, 2015
Replies: 2
Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations)
G
Procedure to define Signing Authority for Procurement Limits
Started by Gumby24
Apr 13, 2015
Replies: 2
ISO 13485:2016 - Medical Device Quality Management Systems
P
Can a company define new quality standards for special industry
Started by petersool
Jan 13, 2015
Replies: 2
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
L
Are there any requirements to define barcode requirements ?
Started by LesPiles
Oct 23, 2014
Replies: 2
Misc. Quality Assurance and Business Systems Related Topics
X
How to define Calibration Acceptance Criteria
Started by xixide
Oct 7, 2014
Replies: 3
General Measurement Device and Calibration Topics
H
ISO 17025 - How to define a "Test Equipment" ?
Started by Hanr3
Sep 3, 2014
Replies: 2
ISO 17025 related Discussions
J
Where do you define Internal Auditor qualifications?
Started by Jim-S
Jun 9, 2014
Replies: 9
Internal Auditing
V
Is there an approach to define the "must 'or' should" in supplier audits?
Started by v9991
Apr 20, 2014
Replies: 2
US Food and Drug Administration (FDA)
T
Internal Audit - How to define the Importance of Departments and Processes
Started by tomate
Feb 5, 2014
Replies: 8
Internal Auditing
T
Help me understand how to define Processes
Started by thira7
Jan 21, 2014
Replies: 40
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
L
How to define R & D Receiving (Incoming) Inspection Plan
Started by lisawxf80
Dec 26, 2013
Replies: 18
Design and Development of Products and Processes
B
How to define and implement Configuration Management
Started by bhavya vee
Mar 8, 2013
Replies: 5
Document Control Systems, Procedures, Forms and Templates
C
How to Define and Document Controls of Outsourced Processes
Started by charu13
Feb 7, 2013
Replies: 5
Food Safety - ISO 22000, HACCP (21 CFR 120)
S
Please help me define training requirements for a Career in Regulatory Affairs
Started by SGquality
Nov 10, 2012
Replies: 2
21 CFR Part 820 - US FDA Quality System Regulations (QSR)
K
How to define the Acceptances Criteria for all equipment?
Started by Kenneth_1217
Oct 13, 2012
Replies: 7
Manufacturing and Related Processes
L
Definition
Program - How do you define Program with regard to ISO 9001?
Started by LesPiles
Jun 20, 2012
Replies: 3
Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically
A
Supplier Evaluation SOP - How do I Define Major and Minor Suppliers?
Started by Asant
May 22, 2012
Replies: 14
Supplier Quality Assurance and other Supplier Issues
Q
Where to define Authorities and Responsibilities in Documentation?
Started by QAMTY
Apr 2, 2012
Replies: 1
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
J
Define Energy Used/Delivered - Applicable to Electrical or Mechanical Power or both?
Started by jscholen
Mar 6, 2012
Replies: 1
21 CFR Part 820 - US FDA Quality System Regulations (QSR)
R
820.50 (A) (2)Define the Type and Extent of Control to be exercised over Vendor
Started by RobertP45
Feb 28, 2012
Replies: 5
Misc. Quality Assurance and Business Systems Related Topics
A
Where to define Process Tailoring Form used in CMMI in the ISO 9001 Quality Manual?
Started by arunnivaz
Feb 7, 2012
Replies: 5
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
Q
Criteria to define QMS processes in ISO/TS 16949:2009
Started by qusys
Nov 16, 2011
Replies: 23
IATF 16949 - Automotive Quality Systems Standard
S
How to define New Equipment? Device is Returned, Refurbished or Repaired
Started by SMCM94
Oct 18, 2011
Replies: 3
Misc. Quality Assurance and Business Systems Related Topics
C
Controlling Documents: Beyond the standard, how do we truly define what to control
Started by cafoltz
Sep 28, 2011
Replies: 9
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
C
How to define Process Special Characteristics (SC)
Started by cqt18060180
Sep 14, 2011
Replies: 4
FMEA and Control Plans
What is the meaning of "define/defined" in ISO 9001?
Started by kedarg6500
Aug 19, 2011
Replies: 19
ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards
Local Control Document procedure....define it or not?
Started by Crusader
Aug 3, 2011
Replies: 24
Document Control Systems, Procedures, Forms and Templates
M
Excel Templates for Plan & Define Phase in NPI Process for Tire Manufacturer
Started by Mati127
May 13, 2011
Replies: 1
Excel .xls Spreadsheet Templates and Tools
R
Define Data from Taguchi to Response Surface Methodology in Minitab
Started by RIDZWAN RAHIM
May 12, 2011
Replies: 2
Using Minitab Software
K
How to define PVC Pellet Quality
Started by KCIPOH
Apr 26, 2011
Replies: 8
Manufacturing and Related Processes
Share:
Twitter
Pinterest
WhatsApp
Email
Link
Forums
Common Quality Assurance Processes and Tools
FMEA and Control Plans
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to the use of cookies.
Accept
Learn more…
Top
Bottom