Script of R software to conduct Nested GRR for Destructive Testing

Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
O Importing Data via Script - Assign Column as Text (Minitab) Using Minitab Software 3
O Minitab Script to Save Regression Plots to an Image File Using Minitab Software 8
R Minitab Multiple Regressions Script Help Using Minitab Software 1
R Shall a new UDI-DI be required when stand-alone software device's version is updated? EU Medical Device Regulations 1
R MSA for ATE (Automatic Test Equipment Embedded Software) Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 5
S MDR GSPR Clause 17 - Software Requirements EU Medical Device Regulations 2
L Turkish Requirements - Does the Software need to be translated? CE Marking (Conformité Européene) / CB Scheme 2
MDD_QNA Medical Device Software - Is a Help Button required? IEC 62304 - Medical Device Software Life Cycle Processes 1
F Software as a Medical Device (SaMD) Technical File Requirements Manufacturing and Related Processes 1
D Software User Interface Languages for LVD and IVD CE Marking (Conformité Européene) / CB Scheme 2
A Software as Medical Device (SaMD) definition and its applicability Other Medical Device and Orthopedic Related Topics 4
K Software Validation for Measurement Tools used in Process Validation ISO 13485:2016 - Medical Device Quality Management Systems 2
B ISO 14971 Applied to Software ISO 14971 - Medical Device Risk Management 2
N ERP Software Implementation Manufacturing and Related Processes 3
C NCR (Nonconformance System) Software Nonconformance and Corrective Action 7
U Document Approval - Software company ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
B Risk Assessment Checklist for Non product Software IEC 62304 - Medical Device Software Life Cycle Processes 1
MrTetris Should potential bugs be considered in software risk analysis? ISO 14971 - Medical Device Risk Management 5
S SOP for ISO 13485:2016 Quality related Software validation ISO 13485:2016 - Medical Device Quality Management Systems 8
J Designing new gauge tracking software IATF 16949 - Automotive Quality Systems Standard 4
T First 510(k) submission - Class II software as medical device US Food and Drug Administration (FDA) 1
B Notified Bodies for Software (MDR) EU Medical Device Regulations 1
C MDR - Question around software accesories EU Medical Device Regulations 2
S Software for Supplier Charge back and internal PPM General Information Resources 2
G Assignable cause/corrective action list for SPC Software Statistical Analysis Tools, Techniques and SPC 3
K ERP System Software Validation - ISO13485 2016 4.1.6 Design and Development of Products and Processes 8
S Recommendation for user friendly Gaga R&R and Cpk software Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 10
M HR (Human Resources) based software recommendations Human Factors and Ergonomics in Engineering 2
V Gage Management and Gage R&R Software General Measurement Device and Calibration Topics 1
F Medical Devices-South Africa _Post approval changes and Software Other Medical Device Regulations World-Wide 0
Marc Security in Health Industry Software - February 2020 IEC 27001 - Information Security Management Systems (ISMS) 0
D Software validation in Medical Equipment Other Medical Device and Orthopedic Related Topics 20
C Experience with Agile PLM (Product Lifecycle Management Software) software from Oracle? Document Control Systems, Procedures, Forms and Templates 3
JoCam Software Translation under MDR requirements EU Medical Device Regulations 5
W Air Quality Measurement Hardware and Software General Measurement Device and Calibration Topics 11
Q Is that any difficulty to do software DFMEA and PFMEA in ISO 13485? ISO 13485:2016 - Medical Device Quality Management Systems 5
F Management of Software version while NB reviews Technical file CE Marking (Conformité Européene) / CB Scheme 7
C QMS Document Management Software Recommendations Quality Assurance and Compliance Software Tools and Solutions 15
Q Software SOP - Use and maintenance of an ERP system Software Quality Assurance 4
Z Software Library - could it be a medical device? ISO 13485:2016 - Medical Device Quality Management Systems 5
B HIGH QA Software - Auto ballooning software Quality Assurance and Compliance Software Tools and Solutions 2
E In need of a new TGA sponsor - Small software company Other Medical Device Regulations World-Wide 4
I Custom software services to be used by medical software ISO 13485:2016 - Medical Device Quality Management Systems 1
S Examples of software changes that required a 510k US Food and Drug Administration (FDA) 2
S Best software for customer support/complaints? Customer Complaints 0
D Reduction of software class based on multiple external risk controls IEC 62304 - Medical Device Software Life Cycle Processes 5
M Informational TGA – Submissions received: Regulation of software, including Software as a Medical Device (SaMD) Medical Device and FDA Regulations and Standards News 1
B Does EN ISO 15223-1:2016 include the graphic symbols to be added to software and IFU? Other Medical Device Related Standards 9
G Strategy for IEC62304 implementation half way into the software development process IEC 62304 - Medical Device Software Life Cycle Processes 9
F Software development plan for SW update IEC 62304 - Medical Device Software Life Cycle Processes 2
Similar threads


















































Top Bottom