Information about MSA (measurement systems analysis) software

B

BAQUEROJ

#1
hi i`m jose from Ecuador i new in this foro and I need an Msa software but the ones that i found are too simple could you help me with some page where i can find a complete msa sofware....
 
Elsmar Forum Sponsor

Jim Wynne

Leader
Admin
#2
Re: Information about MSA software

hi i`m jose from Ecuador i new in this foro and I need an Msa software but the ones that i found are too simple could you help me with some page where i can find a complete msa sofware....
Welcome to the Cove :D

I've used Cybermetrics GAGEtrak in the past. It's a full-featured calibration and MSA program. I can't vouch for the latest versions, nor do I have any interest in the company. You can download a free 30-day trial here and try it out for yourself.
 
B

BAQUEROJ

#3
Thanks but i have a question in this software i could calculate bias linearity stability and r&r of my measure system?????....
 

Stijloor

Leader
Super Moderator
#6
Thanks but i have a question in this software i could calculate bias linearity stability and r&r of my measure system?????....
According the features sheet it is compliant with:
Gage R&R (MSA Third Edition Suite)
So I assume it does the things you want. But why not follow Jim's advise and give it a free try?

Stijloor.
 

Miner

Forum Moderator
Leader
Admin
#7
It is more expensive, but Minitab has a full-featured set of MSA analyses, including Attribute studies, not to mention many other statistical analyses.
 
Thread starter Similar threads Forum Replies Date
A Loss of certification because of outdated information in the Clinical Evaluation Report CE Marking (Conformité Européene) / CB Scheme 8
I Request for information regarding remote medical monitoring software (its technical documentation and the IUD system) IEC 62304 - Medical Device Software Life Cycle Processes 2
R Finding Equivalent Material Information Manufacturing and Related Processes 1
A Information on Process-based Internal Auditing Needed Internal Auditing 6
G Confidentiality of information during MD registration worldwide Other Medical Device Regulations World-Wide 0
S Risk control through Information for safety ISO 14971 - Medical Device Risk Management 8
B Documented information - Should be controlled? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
J PQ Systems User Community information? Using GAGEpack Software 12
B PSW - Organization Manufacturing Information APQP and PPAP 0
H Do you repeat information throughout your documentation submission? EU Medical Device Regulations 4
A Can a organization use a disclaimer "pending AS9100 Certification" in Marketing Information? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
D FDA Information - Revising the Instructions for Use US Food and Drug Administration (FDA) 0
M Need Help With Information Security Asset Risk Register IEC 27001 - Information Security Management Systems (ISMS) 2
S Mechanical Test Under FDA Freedom of Information Act Medical Device and FDA Regulations and Standards News 5
Watchcat Summary of De Novo Biocompatibility Information, 2015-2018 Other US Medical Device Regulations 0
Q Self-assessment audit information Quality Management System (QMS) Manuals 6
Sidney Vianna Release of ISO 10013:2021, Quality management systems – Guidance for documented information Other ISO and International Standards and European Regulations 0
W How long do you keep information about equipment no longer used? Document Control Systems, Procedures, Forms and Templates 2
L Documented Information in Internal Audits Process (9.2) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
R What information do i need to get from the device manufacturer 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
T Types of confidential information ISO 17025 related Discussions 8
D Preservation of Electronic Data / Information Technology ISO 13485:2016 - Medical Device Quality Management Systems 5
SANTHSH API Spec.Q1 Standards Version in Purchasing Information Oil and Gas Industry Standards and Regulations 1
eule del ayre Documented Information - Periodic Review of Documents? IATF 16949:2016 / ISO 9001:2015 IATF 16949 - Automotive Quality Systems Standard 34
R Information on obtaining a market authorization for China China Medical Device Regulations 2
B SN95 Respirator Approval Information Other Medical Device Related Standards 0
R Risk assessment on IT containers and the information they contain IEC 27001 - Information Security Management Systems (ISMS) 4
O EN 301 489-1 and EN 301 489-17 - Where do we get the information of the Published versions? CE Marking (Conformité Européene) / CB Scheme 1
K Article 18: Implant Card and information to be communicated. EU Medical Device Regulations 5
K EU MDR Annex 1 Chapter III: Information in the Instructions for Use-23.4 (e) the performance characteristics of the device; EU Medical Device Regulations 2
Q GMDN Registration Basic preliminary Information EU Medical Device Regulations 0
J Controlled information versus defined documents / records ISO 13485:2016 - Medical Device Quality Management Systems 3
A Medical device Reporting : Good Faith Effort for Additional information Other US Medical Device Regulations 2
P Cenelec updated standard information CE Marking (Conformité Européene) / CB Scheme 1
Richard Regalado Automotive News TISAX - VDA ISA (information security assessment) VDA Standards - Germany's Automotive Standards 7
JoCam False information provided for Medical Device Registration - What are the implications? Other Medical Device Related Standards 3
adir88 Information of safety can reduce risk now? ISO 14971 - Medical Device Risk Management 12
Richard Regalado What could go wrong with information: Ransomware statistics and facts (2018 to present) IEC 27001 - Information Security Management Systems (ISMS) 0
Q LOT or Serial Number Symbol not used when the information is contained in the UDI? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
A Information about Medical Device Test Laboratories Other Medical Device and Orthopedic Related Topics 4
C Missing routers/documented information Nonconformance and Corrective Action 5
MrTetris Unacceptable risk and information for safety ISO 14971 - Medical Device Risk Management 16
M Is Harmonised EN 1041 (Information Supplied By Manufacturer) Worth Looking At? EU Medical Device Regulations 7
P Predicate Device Information for 510(k) Submission Medical Device and FDA Regulations and Standards News 4
V IS/ISO/IEC 17025:2017 Clause 7, sub clause 7.11 Control of data and information management ISO 17025 related Discussions 1
A Medical Device Contract Manufacturing Requirements and Information - Help wanted ISO 13485:2016 - Medical Device Quality Management Systems 5
H Analog Pressure Gauge with no EN837 accuracy class information General Measurement Device and Calibration Topics 5
M Informational EU – MDCG 2019-12 Designating authority’s final assessment form: Key Information Medical Device and FDA Regulations and Standards News 0
G What information to put on measurement Dimensional Results APQP and PPAP 7
L MDR - Information in the instructions for use - clause 23.4.(z) EU Medical Device Regulations 4

Similar threads

Top Bottom