
Certificates of Analysis: Don’t Trust, Verify
Taking vendor product data at face value puts pharmaceutical manufacturers and their supply chain partners at risk.
Good read:
Last edited:
Follow along with the video below to see how to install our site as a web app on your home screen.
Note: This feature may not be available in some browsers.
Some thoughts/suggestions for discussion after looking around here.
Realistic, overkill, get what you pay for, don't care?
Would like to hear members' thoughts, counterpoints, etc. especially on cost vs quality. The path to quality is known. Will people pay or too much for UGL customers?
=======
Every Source should provide with each shipment ...
1. 3rd party C of A on finished product batch specific to that shipment
- endotoxin screen
- metals with ICP
- purity(ies) / concentration(s) using hplc plus ms (or gcms)
2. C of A for bulk api for each batch (hplc plus ms or gcms) upon request.
Of course Sources would do themselves a big favor if they screened for impurities as well as purity on the APIs (aka raws) upfront so no surprises on the finished batches. First things first.
There should never be any surprises with a batch. Completely addressable.
And please clean up the product listings...
1. mg is not a unit for API concentration. Use mg/ml.
If I see 200 mg listed and later on a mention that it is a 10 ml vial I am going to assume your stuff is drastically underdosed. That should be clear to you to.
Best practice is listing the API concentration plus the total API per total vial volume.
Example: 300 mg/ml (3000 mg per 10 ml)
2. Denote volumes (ml) for finished vials. People don't want to guess.
3. List the oil used for injectables and also the excipients/preservatives used plus their concentrations.
What is this deal with not disclosing what is in the vial? You don't know, or is it a trade secret lol? Come on.
4. Spend at least as much time assuring your customer you know basic chemistry as you spend on the beautiful packaging design and gimmicks/marketing.
Be the change.
======
Is this a template Meso should endorse for Sources? Even daylighting the concepts with a suggested template would go a long way to educate consumer and further harm reduction initiative IMO.
Liska and Rido love me. That is all that matters.Wish I could downvote this peace of crap question more than once….who would ever think of posting such a dumb idea … go back to Reddit you loser… you only joined in October and you already know this much? Who are you? bigboost22 hiding in disguise? Get a job loser….
Jk bud. But I finally made my way over here from the link you shared and saw you got roasted too lol. Your idea wasn’t that bad though….
Hope you’re having a good Christmas
How long does it take to get reaction powers in the underground… I can’t react only comment.Liska and Rido love me. That is all that matters.
Never been on reddit. Do have a few posts at ExcelMale and TNation.
You too Brother DW!
Perhaps one of the vets can answer. Must be a seniority perk for higher rank or some other attribute. I don't have that option either. My 10k posts and likes on those other sites does me no good here. Starting from scratch. A clown as Rido says haha.How long does it take to get reaction powers in the underground… I can’t react only comment.
Perhaps one of the vets can answer. Must be a seniority perk for higher rank or some other attribute. I don't have that option either. My 10k posts and likes on those other sites does me no good here. Starting from scratch. A clown as Rido says haha.
I like your can do attitude and goal orientation.
Edit: wait a minute I just noticed I do have it now. So must he a few hundred posts and 200 or so likes.
I’m sure you’ll know the exact minute I get mine then… il make it very well known…Edit: wait a minute I just noticed I do have it now. So must he a few hundred posts and 200 or so likes.
I agree with you on the compounding pharmacies.There are large compounding pharmacies in US who refuse to share C of A for APIs and ingredient listing with amounts for specific batches with customers. To me that is a big reg flag.
The line between compounding pharmacies and UGL seems to blur more each day. Take the current semaglutide situation. Where do you think compounders are sourcing semaglutide? I am pretty sure it isn't from Novo.
What specifically do you disagree with?For the record I will respectful disagree with @Millard on above. Once the scope of tests is properly defined then it is as simple as sending the analytical lab extra sample as needed (samples are being sent routinely anyway for APi purity). Of course it would helpful to validate this process with multiple analytical labs (have two independent labs tell you the same thing ). Currently that is a work in progress.
There may be some proof of method developement/scoping work we would need to do with @janoshik (as example) in identifying utility of gcms vs hr-lcms for impurity profiling.
Thanks for your comments. I know you want more testing. That is not it.What specifically do you disagree with?
Is it that I think it is impractical and unrealistic to expect the realization of this for every AAS-related product sold by UGL sources on the black market at this time?
Is it that I am doubtful that most consumers will pay what could be significantly higher prices?
I don't think it is practical/realistic for many reasons, the least of which is market forces.
OR
Is it that you think I don't want more testing by UGL sources?
Because I most certainly do want to see more comprehensive testing.
I would love to see same US government regulations/testing applied to illicit UGL manufacturing as legal pharmaceutical manufacturing. Well, that's just not going to happen.
That doesn't mean UGL consumers should do nothing. I've strongly advocated more product testing for years.
I think the community has make great progress in requiring at least some analytical testing by UGLs. Consumers primarily want to know how much active ingredient they are getting.
Most UGLs perform this type of analytical testing of select products. I think it is realistic and practical to pressure these UGL to perform this type of testing on every batch of every product. We're not there yet, the community pressure is strong and the trend is looking good.
I applaud your efforts to compel the community to pressure UGL sources/manufacturers to perform more testing.
What I would enjoy seeing is the specific costs of the additional testing your are recommending in your proposal. Obviously, multiplying this figure by the number of unique items produced by the UGL. And if you want testing from multiple analytical labs, then multiply the costs by that number too.
Only then can we begin to see how realistic/practical this proposal would be.
Love your comments. Seriously. Which leads me to ask the following question?I’m all for more testing but let’s take a deeper look into this situation.
I know you’ve been on boards for a while but I’m not sure you understand how some of these UGLs work. Have you seen the photos of some of these labs that have been busted? There was a guy brewing in a tent with a box fan for ventilation. Another guy was brewing Tren in gallon milk jugs while grilling steaks. Hell, look at the most recent bust in Poland. He was storing plastic jugs of oils under his bathroom sink. Do you really think a lab testing showing 2% impurities is going to deter someone from ordering?
I’m not knocking your idea at all but the UGL is a different market. There’s guys here buying bottles of test for $8-12 dollars. Vials that have shown to have floaters on them but they’re still begging for more.
There’s 2 types of people on Meso. Guys who run Pharma and guys who run UGL. The guys running UGL know what they’re paying for. If they were concerned about heavy metals or impurities they’d run pharma. Shit 90% of the guys on here don’t even test their own gear.
Agree. Which is why some dudes pay $15-20 per amp of Bayer Rimos from Turkey… or guys will paying $90 for a 200mg/10ml vial lol.Sad to say there is no Pharma / compounded Pharma methenolone available for instance in US
Agree. Which is why some dudes pay $15-20 per amp of Bayer Rimos from Turkey… or guys will paying $90 for a 200mg/10ml vial lol.
It’s nice that labs are actually posting some photos of their equipment and setups. I also thinks it’s great Millard made it a requirement for all new sources to post lab tests before coming to Meso. Years ago on Eroids we relied on Chinese HPLC reports that always showed 99% purity.
Pharma companies are great. I’ve sent them pictures of their products I’ve seen on here and they’ll confirm if they’re authentic or not. Safe to say there’s a lot of counterfeit Pharma amps being sold by some fellas here.And to be fair this (not providing C of A, batch data, impurity testing, etc) isn't just a UGL issue. One of my go to tests with compounders is to ask them the exact same questions I pose above. It is a great litmus test for their integrity. The scummy ones hide behind "IP concerns" or Competitive Intel if I ask them for their C of A for USP API they supposedly received from FDA inspected supplier. Some won't even disclose the actual ingredients in the medication they sent me. Fancy that. "Trade secret" LOL. The semaglutide offering currently from compounders is another glaring example. There is ZERO chance that API coming from an FDA inspected site.
But I contact a legit Pharma manufacturer and ask for a batch C of A....guess what? No problem at all. Hence, I think a UGL+/++ model will really benefit Subscribers who go to the trouble. I am sure there are plenty of discriminating anabolic enthusiasts out there willing to pay extra to those who put in the work. How many and how much? I am hopeful we will find out.
And we are back to the methenolone example above. Thanks again for your comments. My intention is constructive and I very much appreciate your constructive comments. I was not a fan of the bathtub GHB in the 90s and I ain't going to change course now. Stubborn. Change requires actions which initially appear unreasonable. History will be the judge. But like I said everyone will learn something in the process regardless.Safe to say there’s a lot of counterfeit Pharma amps being sold by some fellas here.
I also think it is realistic and practical to test for heavy metals and microbial contamination by anyone who wishes to spend the money.I disagree that it is impractical and unrealistic to test for heavy metals and perform non targeted impurity analysis plus basic endotoxin screen for each finished batch. My hypothesis is that it is realistic and practical. I want to make it part of the cost of doing business. Will the customer agree as they become educated with new data?
This is great. You should post more about this. How you would recommend consumers take the initiative and do this themselves? Specifically, what have you found to be the best and most productive way to contact pharmaceutical companies for information about suspected counterfeit pharma products.Pharma companies are great. I’ve sent them pictures of their products I’ve seen on here and they’ll confirm if they’re authentic or not. Safe to say there’s a lot of counterfeit Pharma amps being sold by some fellas here.
The best thing they can do it take pictures and send an email. More than likely you’ll get a response. I just say I was in Turkey/Bulgaria/Iran etc. and picked these up in a pharmacy, are they authentic? I had an old email from Aspen when I sent them pictures of the Karachis with newer exp dates and they confirmed they stopped making that style years ago. That email is from my sourcing account which is closed so I’ll try to find a copy. Below is an email I shot to PanPharma about the counterfeit RotexMedica some sources are offering here.This is great. You should post more about this. How you would recommend consumers take the initiative and do this themselves? Specifically, what have you found to be the best and most productive way to contact pharmaceutical companies for information about suspected counterfeit pharma products.