Software for Supplier Charge back and internal PPM

Elsmar Forum Sponsor

yodon

Staff member
Super Moderator
#2
Most eQMS systems will have a supplier 'module' and can support tracking supplier issues (typically through some supplier corrective action request form / function). I work in medical devices and every system I've worked with has something that can facilitate that aspect

Conversely, none of the ones I've worked with have a means for managing chargebacks. Not to say that none do; I just haven't seen any (which may well be related to my scope being limited to medical devices)
 

Sagwa

Registered
#3
Most eQMS systems will have a supplier 'module' and can support tracking supplier issues (typically through some supplier corrective action request form / function). I work in medical devices and every system I've worked with has something that can facilitate that aspect

Conversely, none of the ones I've worked with have a means for managing chargebacks. Not to say that none do; I just haven't seen any (which may well be related to my scope being limited to medical devices)
Thank you for your reply. We will start using QM module in SAP this summer, and hopefully will help us with this.
 
Thread starter Similar threads Forum Replies Date
N Auditing a Software Code Subcontractor (Supplier) ISO 13485:2016 - Medical Device Quality Management Systems 4
M Mobile Medical Platforms - How to deal with Supplier Hardware/Software Changes? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
R Supplier Quality Investigation - Software and Hardware Issues Supplier Quality Assurance and other Supplier Issues 8
A From Supplier Quality Assurance to Software Quality Assurance Software Quality Assurance 5
K Supplier Control: Medical software "module" ISO 13485:2016 - Medical Device Quality Management Systems 3
M What Software is available for Receiving Inspection / Supplier Evaluation Quality Assurance and Compliance Software Tools and Solutions 4
T Supplier Quality Software to help me keep track of molds, tool and dies at suppliers Supplier Quality Assurance and other Supplier Issues 10
T Software Supplier Risk Assessments General Auditing Discussions 0
A Purchaser Assessments of Supplier Software Capability Customer and Company Specific Requirements 5
I Looking for Supplier (Vendor) Assessment software Supplier Quality Assurance and other Supplier Issues 4
S Supplier Tracking Software Supplier Quality Assurance and other Supplier Issues 7
K Software Updates in the Field and ISO scope ISO 13485:2016 - Medical Device Quality Management Systems 0
M Recurrent event analysis software (python) General Auditing Discussions 2
Y UL 1998 Standard: software classes Software Quality Assurance 0
P Need a programmer for QVI's VMS software for optical inspection machine Inspection, Prints (Drawings), Testing, Sampling and Related Topics 0
S IEC 62304 software costs and time Medical Device and FDA Regulations and Standards News 3
S IEC 62304 - Software verification cost IEC 62304 - Medical Device Software Life Cycle Processes 3
Sravan Manchikanti Software Risk Management & probability of occurrence as per IEC 62304 IEC 62304 - Medical Device Software Life Cycle Processes 8
I Form templates for software (iso9001) Document Control Systems, Procedures, Forms and Templates 0
H Software Interface Translation IVD Regulation EU Medical Device Regulations 0
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
M IEC 62304 Software changes - Minor labeling changes on the GUI IEC 62304 - Medical Device Software Life Cycle Processes 3
silentmonkey Rationalising the level of effort and depth of software validation based on risk ISO 13485:2016 - Medical Device Quality Management Systems 10
T Do I need a qualified compiler for class B software? IEC 62304 - Medical Device Software Life Cycle Processes 3
S Manufacturing Execution Systems Software Costs Manufacturing and Related Processes 0
E 13485:2016, Sections 4.1.6, 7.5.6 and 7.6 - Validation of Software - Need some Advice please ISO 13485:2016 - Medical Device Quality Management Systems 2
R Medical Device Software Certification IEC 62304 - Medical Device Software Life Cycle Processes 1
S HIPAA-compliant monitoring software (advice needed) Hospitals, Clinics & other Health Care Providers 0
A Software bug fixes after shipping a product EU Medical Device Regulations 3
J Medical software Patient outcome Medical Information Technology, Medical Software and Health Informatics 2
Y We are Looking for EASA LOA TYPE 1 experienced software developer Job Openings, Consulting and Employment Opportunities 0
F Grand Avenue Software, Q-Pulse or Qualio - which for a full eQMS? Medical Information Technology, Medical Software and Health Informatics 1
K SOUP (Software of Unknown Provenance) Anomaly Documentation IEC 62304 - Medical Device Software Life Cycle Processes 2
Q Storing and developing SAMD (Software as a Medical Device) in the Cloud IEC 62304 - Medical Device Software Life Cycle Processes 3
I Old Time Scatter diagrams for defect type and location- software Quality Tools, Improvement and Analysis 3
SocalSurfer AS9100 new certificate, but need QMS software, help Quality Assurance and Compliance Software Tools and Solutions 2
C Is my software an accessory? Telecommunication between HCP and patients EU Medical Device Regulations 10
K Verify Software Architecture - supporting interfaces between items IEC 62304 - Medical Device Software Life Cycle Processes 1
A What are the pros and cons of using an audit software for internal auditing? General Auditing Discussions 4
A Risk Number for each software requirement IEC 62304 - Medical Device Software Life Cycle Processes 7
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) 9
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

Similar threads

Top Bottom