SBS - The best value in QMS software

What would a After Market Objective and how can it be measured?

Ajit Basrur

Staff member
Admin
#11
Nope. I don't think Customer Satisfaction Survey can effectively capture customers' perception (at least I have not seen one), as always the quantified response is biased and create a lot more questions than answers.

Any objective shall consider financial , customer expectants, internal process capabilities, and learning/growth. Without due considerations to all abovementioned factors, we are destined to fail.
Ernst,

Dont you think that aspects relating to financial, customer expectants, internal process capabilities should be considered upfront before accepting the customer ? If the organsiation thinks they cannot meet these factors, why in the first place the Customer is accepted - should not be, right ?

However i have to come up with a aftermarket objective for my Aftermarket Department. Basically, this department services the client right after sales.
I cannot seem to figure out how to contruct this objective and what would be the measuring tools to measure this objective> anyone out there who can help me.
And the question raised by Cheryl was specifically for a department who have to serve customers after the sales is effected and this types of CSI fit the best. I know you cannot have the "IDEAL" one as the answers vary from an individual to individual but can address the customer expectations to a fair respect.
 
Elsmar Forum Sponsor
E

Ernst Kong

#12
Ernst,

Dont you think that aspects relating to financial, customer expectants, internal process capabilities should be considered upfront before accepting the customer ? If the organsiation thinks they cannot meet these factors, why in the first place the Customer is accepted - should not be, right ?



And the question raised by Cheryl was specifically for a department who have to serve customers after the sales is effected and this types of CSI fit the best. I know you cannot have the "IDEAL" one as the answers vary from an individual to individual but can address the customer expectations to a fair respect.
:topic: Huh, i'm speechless.....almost.:mg:

To my knowledge,any organization, any one , have dreams (or vision, or destination statement, or corporate objectives,,,,etc), any dept./division within that organization MUST contribute to these objectives, hence we have departmental objectives. No company exist solely on customer satisfaction alone (never tell me you are going to please the customers at any cost,ok), it is critical, but there are other considerations, like profit to feed you and your family.

Again, please consider what Jim has said, what the company's need might be? (translation: how can u contribute to the future survival/achievement).It is not about accepting order.

Well, CSI is a good thing, but the survey isn't. Customer Satisfaction Survey is the beginning, not an end. I would never recommend anyone to use rating from a survey as an objective, espeacially so the rating looks vague at best.
 
Thread starter Similar threads Forum Replies Date
M Sample record for verification performed by importers before placing a device on the market EU Medical Device Regulations 0
thisby_ Post Market/Production Risk Assessment ISO 14971 - Medical Device Risk Management 0
R SaMD - Placing on the Market before DoA EU Medical Device Regulations 2
P Clinical Trial Requirement - No equivalent devices in the market CE Marking (Conformité Européene) / CB Scheme 3
D Economic Operators, EU Market Access EU Medical Device Regulations 2
E Medical Device - CE marking - Local market notifications EU Medical Device Regulations 2
D Deciding whether or not pre-market clinical investigation is required for low risk device EU Medical Device Regulations 5
R Information on obtaining a market authorization for China China Medical Device Regulations 2
M EU MDR - Labilities when a device is discontinued from the Market EU Medical Device Regulations 1
A Packaging device with accessories already on the market Other Medical Device Regulations World-Wide 0
S Can a Contract Manufacturer "release" product on behalf of client to the market? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
dgrainger Clue to UK's new regulatory requirements - approval of all devices placed on the market? Other Medical Device Regulations World-Wide 1
F When to market and distribute device in EU? EU Medical Device Regulations 3
N Post Market Surveillance Package Example Wanted ISO 13485:2016 - Medical Device Quality Management Systems 1
T Modification of a product on the market EU Medical Device Regulations 2
M Differences in post market safety reporting for Combination Product Applicants Medical Device and FDA Regulations and Standards News 1
K Product (Device) Life cycle - Product Life AFTER the Post Market Phase Medical Device and FDA Regulations and Standards News 3
M Post Market Surveillance for Class II Medical Devices Medical Device and FDA Regulations and Standards News 2
N "Placing on the market" & "putting into service"- one time regulatory event or Continual supply event? EU Medical Device Regulations 2
H Post-market surveillance strategy EU Medical Device Regulations 2
B Procedures for Complaint Handling and Post Market Surveillance EU Medical Device Regulations 7
A Post-market clinical followup studies (PMCF) EU Medical Device Regulations 16
M Informational Creating a post market surveillance (PMS) system for medical devices – Part 1 Medical Device and FDA Regulations and Standards News 7
E Post Market Surveillance Standard Various Other Specifications, Standards, and related Requirements 4
N When is "placing on the market"? MDD certified medical devices EU Medical Device Regulations 32
K EU MDD Class I Device market access / certification after 26th May 2020 EU Medical Device Regulations 9
T Post-Market Surveillance Plan - Requirements outlined in Annex III (1.1b) EU Medical Device Regulations 2
M Informational Health Canada guidance document – Pre-market Requirements for Medical Device Cybersecurity Medical Device and FDA Regulations and Standards News 0
Y Post Market Surveillance Indicators and Analysis method EU Medical Device Regulations 1
M Post Market Surveillance Plan Template EU Medical Device Regulations 12
F Vietnamese Post-Market Surveillance Requirements for a medical device in Japan Other Medical Device Regulations World-Wide 0
M PMCF (Post Market Clinical Followup)/ PSUR template EU Medical Device Regulations 8
C Shipping Medical Devices to US before pre market clearance US Food and Drug Administration (FDA) 1
M New medical device on the market before MDR EU Medical Device Regulations 12
M Informational The ANSM decides, as a precautionary measure, to withdraw from the market macrotextured breast implants and breast implants with polyurethane-coated s Medical Device and FDA Regulations and Standards News 0
S PMCF (Post Market Clinical Followup): Rationale for Exemption - Software Medical Devices EU Medical Device Regulations 6
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
S Post Market Surveillance and Annual Product Review in ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 2
M Informational TGA – Q&A: Use of market authorisation evidence from comparable overseas regulatory bodies for medical devices Medical Device and FDA Regulations and Standards News 0
K Post Market Clinical Follow up and CE Marking for Class IIb medical X-Ray products CE Marking (Conformité Européene) / CB Scheme 1
M Informational Links to recognized / harmonised / consensus Standards for each market Other Medical Device Related Standards 5
M Entering the Italian Market - Implantable Medical Device EU Medical Device Regulations 1
M Informational EU Review and assessment of market surveillance activities 2014-2016 – Medical devices sector Medical Device and FDA Regulations and Standards News 0
M Medical Device News Health Canada – Consultation: Pre-market Requirements for Medical Device Cybersecurity Medical Device and FDA Regulations and Standards News 0
M Medical Device News Joint Action On Market Surveillance Of Medical Devices (JAMS) Releases Progress Update EU Medical Device Regulations 0
M Medical Device News Health Canada Notice of intent: Strengthening the post-market surveillance and risk management Canada Medical Device Regulations 1
S CE ETA (A2) Audit - CE mark for the european construction market CE Marking (Conformité Européene) / CB Scheme 0
M Medical Device News EU - List of national market surveillance authorities by sector and country EU Medical Device Regulations 0
H Claiming equivalence with the product that was sold earlier in the market but not now EU Medical Device Regulations 1
C Spares Market Supplier - Do we need to follow AS9110 or AS9100? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1

Similar threads

Top Bottom