Lab Testing & Certificate of Analysis

Quality · Testing & Verification

Every batch tested. Ask us for the paperwork.

Anyone can print "third-party tested" on a label. The question worth asking is which laboratory, to what standard, and whether they will show you the certificate for the pot in your hand. Here is our answer to all three.

ISO/IEC 17025 accredited lab Every production batch COA on request UK manufactured

Vitality Supplements lab testing and Certificate of Analysis — summary

Vitality Supplements has every production batch tested by an independent third-party laboratory holding ISO/IEC 17025 accreditation, the international standard for the competence of testing and calibration laboratories. A Certificate of Analysis, commonly abbreviated to COA, is the document recording the test results for one specific batch. Because a COA is batch-specific, a certificate for one batch does not describe any other batch. Customers can request the Certificate of Analysis for the batch they hold by emailing info@vitality-supplements.co.uk quoting the batch number printed on the pack. Testing covers identity, active content or potency, heavy metals and microbiological safety. ISO/IEC 17025 accreditation applies to laboratories and is a different thing from GMP, which is a manufacturing standard, and different again from a manufacturer testing its own products in house, which is not third-party testing. Vitality products are manufactured in the United Kingdom. Vitality does not use the term GMP on its product labelling.

The Standard

What ISO/IEC 17025 actually means.

"Third-party tested" is an unregulated phrase. It can mean a laboratory with international accreditation ran a full panel — or it can mean somebody once sent a sample somewhere. Both sentences read identically on a label.

ISO/IEC 17025 is the international standard for the competence of testing and calibration laboratories. A laboratory holding it has been independently assessed on its methods, its equipment calibration, the competence of its staff, and its ability to produce results that are valid and repeatable. It is audited, not self-declared.

Every Vitality production batch is tested by an independent laboratory holding that accreditation. Not the first batch, not a representative sample once a year. Each batch.

Three things people confuse

Term What it applies to What it does not tell you
ISO/IEC 17025 The laboratory doing the testing Nothing about how the product was manufactured
GMP The manufacturing facility and its processes Nothing about whether the finished batch was independently tested
"In-house tested" The manufacturer testing its own output It is not third-party testing, whatever else it may be
Why we don't print GMP on our packs

We deliberately keep the term GMP off our labels. It is widely used in supplement marketing in ways that imply an independent certification that the wording alone does not establish. We would rather state something narrower and verifiable — that an accredited third-party laboratory tested the batch — than something broad and impressive that a customer cannot check. If you see GMP on any Vitality pack or product page, it is an error and we would like to know about it.

The Panel

What gets tested.

Testing falls into four areas. Which specific methods and limits apply depends on the ingredient — a mushroom extract and a mineral salt are not checked for the same things.

01
Identity
Confirming the material is what it is supposed to be. This matters more than it sounds — adulteration and substitution are the most common problems in botanical ingredients, where a cheaper plant stands in for an expensive one.
02
Potency & active content
Verifying the stated amount of the active is actually present. This is the number on the front of the pack, checked rather than assumed.
03
Heavy metals
Lead, arsenic, cadmium and mercury. Plants take up whatever is in the soil they grew in, so botanical ingredients need this check regardless of how clean the supply chain looks on paper.
04
Microbiological safety
Total counts plus specified organisms such as Salmonella and E. coli. Particularly relevant for anything fermented, fungal or plant-derived.

The specific parameters, methods and limits applied to any given batch are recorded on that batch's Certificate of Analysis.

Your Batch

Ask for the certificate. We'll send it.

A Certificate of Analysis is batch-specific. That is the whole point of it. A COA describes one production run and tells you nothing about any other — so a brand publishing a single certificate from 2023 as a permanent trust badge is showing you something close to meaningless.

We would rather send you the certificate for the batch you actually own. Every pack carries a batch number.

01
Find your batch number
Printed on the pack alongside the best-before date.
02
Email it to us
Send the product name and batch number to info@vitality-supplements.co.uk.
03
We send the COA
You get the certificate covering that specific batch — not a generic sample document.
Request the COA for your batch.

Send us the product name and the batch number printed on your pack, and we will send the Certificate of Analysis covering it.

Request a COA
How To Read One

What to look for on any COA.

Most people have never been shown how to read one of these. It applies to any brand's certificate, not just ours — and it is the fastest way to tell a real document from a decorative one.

Is there a batch or lot number?
And does it match the number on the pack in your hand? If there is no batch number, the document describes nothing in particular.
Is the laboratory named?
An anonymous certificate cannot be verified. A named laboratory can be looked up.
Is there a date?
A certificate from several years ago tells you about a batch that has long since been consumed.
Are methods stated?
Real certificates name the analytical method used for each parameter — HPLC, ICP-MS and so on — not just a result.
Are specifications shown next to results?
A result of "0.3" means nothing without the limit it is being measured against. Look for a specification column and a pass or fail.
Does it cover the finished product?
Some brands show a COA for the raw ingredient they bought in, not for the capsule they sold you. These are not the same document.
The last one catches most people

A raw-material certificate from an ingredient supplier is easy to obtain and proves the powder was tested before it was blended, encapsulated and packed. A finished-product certificate proves what ended up in the capsule. If you are comparing brands, that distinction is worth asking about directly.

Restraint

What testing doesn't prove.

Testing tells you what is in the capsule. It does not tell you what the capsule will do. Those are separate questions, and conflating them is one of the more common moves in supplement marketing.

A Certificate of Analysis confirms identity, content and safety parameters for a batch. It is not evidence of a health benefit, and we do not present it as one.

Several ingredients we sell — including quercetin, alpha lipoic acid and L-ergothioneine — have no authorised UK or EU health claims at all. Where that is the case, we describe composition and leave it there. Our editorial standards set out how we handle this across the site.

Glossary

The terms, defined.

Certificate of Analysis (COA)
A document recording laboratory test results for one specific production batch.
ISO/IEC 17025
The international standard for the competence of testing and calibration laboratories. Applies to the lab, not the product.
Batch / lot number
The identifier for a single production run, printed on the pack and used to match it to a COA.
Specification
The acceptable range or limit a result is measured against. A result without a specification is uninterpretable.
HPLC
High-performance liquid chromatography — a common method for identifying and quantifying compounds.
ICP-MS
Inductively coupled plasma mass spectrometry — the usual method for measuring heavy metals at trace levels.
Adulteration
Substituting or diluting an ingredient with something cheaper. Identity testing is what catches it.
Finished-product testing
Testing the packed product rather than the raw ingredient that went into it.
FAQs

Testing questions.

Email info@vitality-supplements.co.uk with the product name and the batch number printed on your pack. We will send the certificate covering that specific batch.
A document recording the laboratory test results for one specific production batch. It typically lists each parameter tested, the method used, the specification and the result. Because it is batch-specific, a COA for one batch does not describe another.
It is the international standard for the competence of testing and calibration laboratories. A lab holding it has been independently assessed on its methods, equipment calibration, staff competence and ability to produce valid, repeatable results. It applies to the laboratory, not to the product or the factory.
No. GMP refers to manufacturing practice — the facility and its processes. ISO/IEC 17025 refers to the competence of a testing laboratory. A product can be made in a facility following GMP and never be independently tested, and vice versa. We do not use the term GMP on our labelling.
Every production batch is tested. This is the distinction worth asking any brand about — testing one batch and citing it indefinitely is a very different practice from testing each run.
Identity, active content, heavy metals and microbiological safety. The specific methods and limits vary by ingredient and are recorded on each batch's certificate.
Because certificates go out of date the moment a new batch is made. A wall of PDFs looks reassuring but most of them describe stock that is no longer on shelves. Sending you the certificate for the batch you actually hold is more useful than publishing a hundred that mostly do not apply to you.
In the United Kingdom. Ingredients are sourced from a range of origins, as is normal across the industry; the manufacturing and packing happen in the UK.
No, and we would not claim it does. Testing establishes what is in the capsule and that it meets safety specifications. It says nothing about physiological effect. Several ingredients we sell have no authorised UK or EU health claims, and for those we describe composition only.
About this page

Written by the Vitality Supplements Editorial Team. This page describes our own testing practice, so treat it as what it is — a statement from the brand. The parts you should not have to take on trust are the ones you can check: request the Certificate of Analysis for your batch and read it against the criteria above. The section on how to read a COA applies to any brand's certificate, including those of our competitors. See our editorial standards.

Food supplements should not be used as a substitute for a varied, balanced diet and a healthy lifestyle. This page describes testing and quality practice only and makes no health claims. Laboratory testing establishes composition and safety parameters; it is not evidence of any physiological or health effect. Certificates of Analysis are batch-specific and are provided on request for the batch identified by the number printed on your pack. If you are pregnant, breastfeeding, taking medication or under medical care, consult a healthcare professional before use. See our full disclaimer.