Product specification can look anything like your products dimensions, the volume, it’s weight, the color and any specific labeling that it may need to meet regulation.
In your specifications you need to ensure that you are as specific as you can possibly be, from specific color palettes to the maximum weight of an electric blender. The more specific you are, the easier it will be for your supplier to meet your specifications.
These specifications will also provide your supplier’s quality control team with a standard/guide to monitor the production of the item appropriately.
This is where the in-house vs outsourced inspection arguments come in.
You need to establish whether an in-house team is fully capable of conducting all of the appropriate tests and reporting that is needed for your product, or whether it will be of greater benefit to outsource the professional expertise to a third party quality provider.
As an importer, you need to ensure that you are up to date with all the latest regulation that is specific to your product.
Are you?
{{cta(‘37580c78-0398-44e8-8f88-7682a9c94777′,’justifycenter’)}}
A critical defect – This is defined when the product may cause possible injury or harm to the end user. This product’s safety is compromised.
A laptop’s battery overheating that when unattended whilst charging can cause fires would be classified as a critical defect.
Where the product in question can cause injury to the end user, this results in product recalls and is hugely damaging to your brand.
A major defect – This is defined when its condition will affect the sale of the product in the marketplace, likely resulting in the end user returning it with dissatisfaction.
A coffee maker that does not heat the water adequately to make a decent, drinkable cup of coffee is classified as a major defect.
This product has caused dissatisfaction amongst its end users and they then return it to the store, likely reviewing the product online, which will have an impact on the future sales of that item.
A minor defect – This is defined when its defect is small, and will not affect its saleability in the marketplace and does not pose any harm or injury on the end user.
Take a wooden coffee table for example. Your quality control teams takes the product through its tests and they come across a scratch underneath the table.This is a scratch that your end user will not see in normal use of the product or may never even see it for that matter. This is what we would classify as a minor defect where this product will still go to market as it will not cause any damage or harm to the end user.
But that’s not all…
What about a sample? I have left obtaining a sample for the end…as some importers don’t require a sample before production. While this is not a necessity, by adding this into your production procedure it can help you significantly reduce product defects that come from your selected supplier and factory. Once you have established the appropriate product requirements, you can then request a sample from your supplier. Once you receive your sample you need to analyze it and ensure that it meets all of your requirements, and then send it back to your supplier with either a confirmation to go ahead with your production, or with a list of further specifications that they need to meet. Well, what happens if it doesn’t meet your requirements? Samples will not always meet your specified product requirements. Often times you can catch this just by holding or looking at the product. But, more often than not a substandard product of will reach the end consumer opening your brand up to severe damage and risk.
Therefore an important question you should be asking your supplier before all this is, how they will go about preventing any quality issues that may arise during your operation?
Understanding how your supplier handles quality pressures and compliance procedures will help define what kind of relationship you have with them.
Before mass production, your supplier needs to provide you with a technical compliance folder (TCF) which must contain full compliance reports from physical safety reports, to chemical safety to electrical safety.
For any missing reports, your sample product will need to go through all of the testing procedures that is required to meet specific levels of compliance for your destination country.
If after being tested and analyzed it does not pass the minimum requirements needed for the product, your factory should be able to provide you with a root cause analysis to address what went wrong and then advise on any corrective or preventive action plan.
From here they will be able to make the adjustments as needed and you may also want them to send you another sample after they have made the adjustments that you specified.
Managing product defects can also be addressed after mass production through a Final Random Inspection to check to filter out any last defects within your products.
Often times samples are drawn after mass production for chemical testing and again during your first shipment and also in the case of a re-order shipment.
Doing chemical tests on samples during these three stages is a way of ensuring that your products are still in compliance as contamination may have occurred on the production line or during your shipment process.
Want to know more about one of our many services? Contact us to find out more information about what API can do for your company today.
Quick Links
Address
Copyright © 1981 – 2022 API. All Rights Reserved.