Evaluation Form - Re-evaluating suppliers for their performance

Raffy

Quite Involved in Discussions
#1
Hi,
Currently we have a form in evaluating our supplier including the service provider, however when we were been audited two months ago, our external auditor recommends that we have to generate another set of form to be used in re-evaluating the supplier for their performance? So far, I have no idea what could be the contents of that form? Please help.
Thanks in advance,
Raffy
 
Elsmar Forum Sponsor

Marc

Hunkered Down for the Duration
Staff member
Admin
#2
The first question is what measureables are you going to use for performance evaluation?
 

Raffy

Quite Involved in Discussions
#4
Hi Marc,

Originally quoted by Marc:

"The first question is what measureables are you going to use for performance evaluation?"


First, we deal on how the supplier would come up with the on time delivery of all materials that was been supplied to us.

Second, percent of materials that passed IQA.

That's all that I can think for now.

Originally quoted by gpainter:

"QUALITY OF PRODUCT DELIVERED,ON-TIME DELIVERY,RESPONSE TO PROBLEMS, ISO REGISTRATION"


I agree with you that it must be the quality of the product that was been delivered. And yet another issue that enlighten my mind, is that how do they respond to problems, with this we send a SCAR (Suppliers Corrective Action Form) however for this times, we request them an 8D for those problems that we have with them.

Thank you Marc, gpainter,

best regards,

Raffy
 
M

massfrompak

#5
Hi,
Currently we have a form in evaluating our supplier including the service provider, however when we were been audited two months ago, our external auditor recommends that we have to generate another set of form to be used in re-evaluating the supplier for their performance? So far, I have no idea what could be the contents of that form? Please help.
Thanks in advance,
Raffy
SUPPLIER SHOULD BE EVALUATED ON THE BASIS OF THEIR CHARACTERISTICS REGARDING.
1-PRICE
2-QUALITY OF PRODUCT
3-LEAD TIME
4-SUPPORT ROLE
5-COMMITMENT TO SERVICE ETC

THANX
AHSAN SALEEM
 
C

celwell11

#8
I like the spreadsheet, but am unable to edit it?? It appears as though everything is locked down?? Any help would be great!
 
Thread starter Similar threads Forum Replies Date
J Simple supplier evaluation qualification process form that includes Risk Assessment Document Control Systems, Procedures, Forms and Templates 2
E Supplier Evaluation Form - Example to evaluation suppliers (criteria) please Document Control Systems, Procedures, Forms and Templates 4
K Supplier Evaluation Form or Template wanted AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 7
A Supplier (Steel Mill supplying ingots) Evaluation form wanted Document Control Systems, Procedures, Forms and Templates 10
A Return Goods Evaluation form Document Control Systems, Procedures, Forms and Templates 3
S Internal Auditor Evaluation form ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 16
H Form to send to a supplier of QC services for their evaluation needed ISO 13485:2016 - Medical Device Quality Management Systems 3
C Training needs of employees - Consultant has idea of an employee evaluation form Training - Internal, External, Online and Distance Learning 1
S Training Evaluation Form - Evaluator feel difficulty to fill this form Training - Internal, External, Online and Distance Learning 12
R SPEC, according to Honda, it's meaning? Sourcing QAV Evaluation Form Statistical Analysis Tools, Techniques and SPC 3
M Auditee Evaluation of Auditors Example, Form or Template General Auditing Discussions 6
T Training Evaluation Form - One-page feedback forms that instructors use Training - Internal, External, Online and Distance Learning 14
B Supplier Evaluation - A Form? What shall be done to Effectively evaluate Supplier? Supplier Quality Assurance and other Supplier Issues 4
P Does anyone has a good Employee Performance evaluation form? Document Control Systems, Procedures, Forms and Templates 2
M MSA Evaluation form Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 0
F Biocompatibility evaluation for Hardware/Interface Components? Other Medical Device Related Standards 1
B Clinical Evaluation Expert Panels - MDR EU Medical Device Regulations 1
T Clinical evaluation of a new medical device EU Medical Device Regulations 0
dgrainger Informational MDCG 2020:13 - Clinical evaluation assessment report template EU Medical Device Regulations 0
S A clinical performance evaluation study with an IVD product as Investagional Use product - Clinical Monitor requirements 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
B AS9100 8.4.1 Supplier Selection/Evaluation criteria and reevaluations AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 13
R Clinical evaluation without clinical data - MDR Article 61(10) EU Medical Device Regulations 6
M Clinical Evaluation Plan vs. PMCF Plan EU Medical Device Regulations 19
K Biocompatibility evaluation of gas pathways Medical Device and FDA Regulations and Standards News 5
T HF testing / Summative evaluation for MDDS class I necessary? Human Factors and Ergonomics in Engineering 2
N Evaluation of service providers Supplier Quality Assurance and other Supplier Issues 2
M Can someone share a scrubbed version of Clinical Evaluation Plan (CEP) EU Medical Device Regulations 2
S EU MDR Annex XIV - Clinical Evaluation Plan - What do these methods mean? EU Medical Device Regulations 12
C Material from outside CER evaluation period CE Marking (Conformité Européene) / CB Scheme 8
DitchDigger IEC 60601-1 subclause 5.1 - Adequate evaluation in lieu of testing IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
S Clinical Evaluation - Is this an ISO 13485:2016 requirement? ISO 13485:2016 - Medical Device Quality Management Systems 4
P SOUP anomaly evaluation for MMA IEC 62304 - Medical Device Software Life Cycle Processes 2
M Informational How to perform a clinical evaluation of medical devices – Part 2 – Level of clinical evidence and what sufficient clinical evidence means Medical Device and FDA Regulations and Standards News 9
P IEC 62304 - evaluation of integration and system testing IEC 62304 - Medical Device Software Life Cycle Processes 4
R Supplier evaluation and business needs in the context of ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 2
U Changes to Internal Processes and Risk Evaluation - Mitigations Risk Management Principles and Generic Guidelines 10
M Informational Work in progress at the FDA for biological evaluation – Color Hazard and RISk calculator (CHRIS) Medical Device and FDA Regulations and Standards News 0
M Informational How to perform a clinical evaluation of medical devices – Part 1 – Overview and sample of activities Medical Device and FDA Regulations and Standards News 0
T EU MDR Article 61- Clinical Evaluation EU Medical Device Regulations 2
pashah Looking for Clinical Evaluation SOP acc. MEDDEV and EU MDR Other Medical Device Related Standards 0
K Supplier re-evaluation (API Q1) Manufacturing and Related Processes 8
B Evaluation of Basic Safety during EMC Immunity or Climate Testing IEC 60601 - Medical Electrical Equipment Safety Standards Series 0
S ISO 10993 Biocompatibility Evaluation - Electronic thermometer Other Medical Device Related Standards 3
D Clinical Evaluation Report - Consultant Recommendations Consultants and Consulting 9
qualprod ISO 9001 Clause 9.1 - Monitoring measurement analysis and evaluation ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
M CER (Clinical Evaluation Reports) updates - Product Codes EU Medical Device Regulations 2
A Medical device CER (clinical evaluation report) training/seminar services EU Medical Device Regulations 2
M Informational US – National Evaluation System for Health Technology Coordinating Center (NESTcc) Solicits Public Comments for Data Quality and Methods Frameworks Medical Device and FDA Regulations and Standards News 0
M Informational IMDRF – Proposed update to Clinical Evaluation documents Medical Device and FDA Regulations and Standards News 0
M Informational MDCG 2019-3 Interpretation of Article 54(2)b – Pre- market clinical evaluation consultation procedure with the involvement of expert panels Medical Device and FDA Regulations and Standards News 0

Similar threads

Top Bottom