I could see this group, or a group... of any origin... as a "Watch-dog"...
(Those have a stamp, but not for approval, only to signify, "Active independent random testing.", which would confirm that they are staying within the certified limits imposed. From a group that is not affiliated or controlled by the actual company. That, a business may pay for, but requires knowledge of the certification limits. EG, testing actual "sold consumer goods", not manufactured floor-processed items.)
You see... ISO standards dictate that records are kept, problems are fixed, and formulations are within a set range.
The WHO only restricts things which implicitly cause harm, or have high potential for leading to harm, while the FDA(in the US) regulates what can and can't be within products and marketing.
There is no real group that acts as a "Watch-dog", or "Keeper". Those groups only re-test when a problem is filed, or when new certification is needed. Any country group can do that. We can do that. We should do that.
This would be like random spot-checking, beyond the governmental control. This coming in the form of demanding access to the "Claimed certification proof", warning of "Expired certifications", and testing random live samples, through an independent lab, using that as an alert for investigation, if there was an issue.
Manufacturing will usually pay for testing once, lock-in a formula that passed, and simply follow those standards until something goes wrong. (Correcting only failure to comply to the "Recipe", they detail in the original testing.) However, as the tattoo industry found-out... manufactures change things, due to cut costs, and don't always follow-up with another test. This is where groups come into play.
These individual groups become the parental figure, whistle-blower, of detected potential issues that deviate from the certified agreement/use for manufacturing. they first contact the company, and that is followed by contact to the appropriate agencies who certified them. (If correction is not made, or proof of correction can not be confirmed.)
Like a "Consumer reports", these groups also give "Home-brewers", a friendly warning, when they may be in possible violation. Completely within the rights of any citizen of any country, as long as the warning is not threatening or in the form of extortion. These "Groups", also provide those "Home-brewers", with the resources they need, to get certification. (If that is a possibility. Usually it is not, and the brewers actually need to have a larger company manufacture for them, as the required equipment is not within any affordable budget. That just makes them a recipe-maker, where the recipe does not infringe on another's copyrights, patents, or trademarks.)
Failure to comply, usually results in a visit form the FDA or WHO, in the form of a cease and desist letter, followed by a court date.
(Those have a stamp, but not for approval, only to signify, "Active independent random testing.", which would confirm that they are staying within the certified limits imposed. From a group that is not affiliated or controlled by the actual company. That, a business may pay for, but requires knowledge of the certification limits. EG, testing actual "sold consumer goods", not manufactured floor-processed items.)
You see... ISO standards dictate that records are kept, problems are fixed, and formulations are within a set range.
The WHO only restricts things which implicitly cause harm, or have high potential for leading to harm, while the FDA(in the US) regulates what can and can't be within products and marketing.
There is no real group that acts as a "Watch-dog", or "Keeper". Those groups only re-test when a problem is filed, or when new certification is needed. Any country group can do that. We can do that. We should do that.
This would be like random spot-checking, beyond the governmental control. This coming in the form of demanding access to the "Claimed certification proof", warning of "Expired certifications", and testing random live samples, through an independent lab, using that as an alert for investigation, if there was an issue.
Manufacturing will usually pay for testing once, lock-in a formula that passed, and simply follow those standards until something goes wrong. (Correcting only failure to comply to the "Recipe", they detail in the original testing.) However, as the tattoo industry found-out... manufactures change things, due to cut costs, and don't always follow-up with another test. This is where groups come into play.
These individual groups become the parental figure, whistle-blower, of detected potential issues that deviate from the certified agreement/use for manufacturing. they first contact the company, and that is followed by contact to the appropriate agencies who certified them. (If correction is not made, or proof of correction can not be confirmed.)
Like a "Consumer reports", these groups also give "Home-brewers", a friendly warning, when they may be in possible violation. Completely within the rights of any citizen of any country, as long as the warning is not threatening or in the form of extortion. These "Groups", also provide those "Home-brewers", with the resources they need, to get certification. (If that is a possibility. Usually it is not, and the brewers actually need to have a larger company manufacture for them, as the required equipment is not within any affordable budget. That just makes them a recipe-maker, where the recipe does not infringe on another's copyrights, patents, or trademarks.)
Failure to comply, usually results in a visit form the FDA or WHO, in the form of a cease and desist letter, followed by a court date.
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