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Independent lab results

Published results from laboratories that tested peptide products they or a study team obtained themselves, failures included. Every row names the laboratory, the method, when the testing was done, what was expected, what was found, and where it was published, so you can check it.

A seller's own certificate is not a source here, and neither is a result nobody can trace. The table shows no prices, no purchase links and no overall score for any seller: a row is one measurement of one product, not a verdict on a company. Data as of October 1, 2026; 12 results. Rules: methodology. Download: lab-results.json.

Results

12 of 12 shown
CompoundSellerMeasureResultOutcomeMethodLaboratoryTestedSource
SemaglutideBiotech Peptidescontent3.86 mg
expected: 3 mg of semaglutide per vial, as labelled
failLC-MSMass Spectrometry Core Facility, Szentágothai Research Centre, University of PécsAugust 2023 to March 20241PMID 39509151; PMID 39093567
SemaglutideBiotech Peptidespurity7.7 %
expected: 99%, as stated on the product label or website
inconclusiveLC-MSMass Spectrometry Core Facility, Szentágothai Research Centre, University of PécsAugust 2023 to March 20242PMID 39509151; PMID 39093567
SemaglutideBiotech Peptidessterilityno viable microorganisms
expected: sterile, per Ph. Eur. 2.6.1 and USP <71>
passUSP-71PharmaValid Ltd microbiology laboratory, Budapest (ISO 14644-1 certified)August 2023 to March 20243PMID 39509151; PMID 39093567
SemaglutideBiotech Peptidesendotoxin<2.1645 EU/mg
expected: no acceptance limit is stated in the source for this product
inconclusiveLALPharmaValid Ltd microbiology laboratory, Budapest (ISO 14644-1 certified)August 2023 to March 20244PMID 39509151; PMID 39093567
SemaglutideSemaSpacecontent2.77 mg
expected: 2 mg of semaglutide per vial, as labelled
failLC-MSMass Spectrometry Core Facility, Szentágothai Research Centre, University of PécsAugust 2023 to March 20245PMID 39509151; PMID 39093567
SemaglutideSemaSpacepurity14.37 %
expected: 99%, as stated on the product label or website
inconclusiveLC-MSMass Spectrometry Core Facility, Szentágothai Research Centre, University of PécsAugust 2023 to March 20246PMID 39509151; PMID 39093567
SemaglutideSemaSpacesterilityno viable microorganisms
expected: sterile, per Ph. Eur. 2.6.1 and USP <71>
passUSP-71PharmaValid Ltd microbiology laboratory, Budapest (ISO 14644-1 certified)August 2023 to March 20247PMID 39509151; PMID 39093567
SemaglutideSemaSpaceendotoxin8.9511 EU/mg
expected: no acceptance limit is stated in the source for this product
inconclusiveLALPharmaValid Ltd microbiology laboratory, Budapest (ISO 14644-1 certified)August 2023 to March 20248PMID 39509151; PMID 39093567
SemaglutideUSChemLabscontent1.34 mg
expected: 1 mg of semaglutide per vial, as labelled
failLC-MSMass Spectrometry Core Facility, Szentágothai Research Centre, University of PécsAugust 2023 to March 20249PMID 39509151; PMID 39093567
SemaglutideUSChemLabspurity8.97 %
expected: 99%, as stated on the product label or website
inconclusiveLC-MSMass Spectrometry Core Facility, Szentágothai Research Centre, University of PécsAugust 2023 to March 202410PMID 39509151; PMID 39093567
SemaglutideUSChemLabssterilityno viable microorganisms
expected: sterile, per Ph. Eur. 2.6.1 and USP <71>
passUSP-71PharmaValid Ltd microbiology laboratory, Budapest (ISO 14644-1 certified)August 2023 to March 202411PMID 39509151; PMID 39093567
SemaglutideUSChemLabsendotoxin<2.8658 EU/mg
expected: no acceptance limit is stated in the source for this product
inconclusiveLALPharmaValid Ltd microbiology laboratory, Budapest (ISO 14644-1 certified)August 2023 to March 202412PMID 39509151; PMID 39093567

Notes on each result

  1. LR-0001: Measured 3.86 mg (SD 0.14) against 3 mg on the label: 28.56% more than labelled, which is the paper's own labelling-accuracy figure. The same method read the genuine Ozempic 1 mg pen at +5.05% over its label. A reader dosing by the label would receive more than intended. Named under the sample-control rule: the study team bought this product itself, and the paper reports its results separately from the other products. Test date: The research letter on this study states that test purchases and analytical testing were performed from August 2023 to March 2024; neither paper gives a date for any individual test.
  2. LR-0002: The paper's purity is semaglutide as a share of the whole powder in the vial (3.86 mg of 50.1 mg), not the chromatographic peptide purity a research-grade '99%' claim usually means; the paper found no peptide-like impurities. So the vial is mostly undeclared non-peptide material, and the two percentages measure different things. The measurement stands; the comparison is not like-for-like. Named under the sample-control rule: the study team bought this product itself, and the paper reports its results separately from the other products. Test date: The research letter on this study states that test purchases and analytical testing were performed from August 2023 to March 2024; neither paper gives a date for any individual test.
  3. LR-0003: Tested by what the paper calls a direct injection technique, under both pharmacopoeias. The paper reports the lyophilised powder free of viable microorganisms at the time of testing; it does not test the vial after reconstitution or storage. Named under the sample-control rule: the study team bought this product itself, and the paper reports its results separately from the other products. Test date: The research letter on this study states that test purchases and analytical testing were performed from August 2023 to March 2024; neither paper gives a date for any individual test.
  4. LR-0004: Reported as below 2.1645 EU/mg by kinetic turbidimetric assay (Ph. Eur. 2.6.14, USP <85>) — an upper bound, not a measured level, although the paper's abstract describes endotoxin as detected in all samples. No limit is stated, so no pass or fail is given here. Named under the sample-control rule: the study team bought this product itself, and the paper reports its results separately from the other products. Test date: The research letter on this study states that test purchases and analytical testing were performed from August 2023 to March 2024; neither paper gives a date for any individual test.
  5. LR-0005: Measured 2.77 mg (SD 0.12) against 2 mg on the label: 38.69% more than labelled, which is the paper's own labelling-accuracy figure. The same method read the genuine Ozempic 1 mg pen at +5.05% over its label. A reader dosing by the label would receive more than intended. Named under the sample-control rule: the study team bought this product itself, and the paper reports its results separately from the other products. Test date: The research letter on this study states that test purchases and analytical testing were performed from August 2023 to March 2024; neither paper gives a date for any individual test.
  6. LR-0006: The paper's purity is semaglutide as a share of the whole powder in the vial (2.77 mg of 19.3 mg), not the chromatographic peptide purity a research-grade '99%' claim usually means; the paper found no peptide-like impurities. So the vial is mostly undeclared non-peptide material, and the two percentages measure different things. The measurement stands; the comparison is not like-for-like. Named under the sample-control rule: the study team bought this product itself, and the paper reports its results separately from the other products. Test date: The research letter on this study states that test purchases and analytical testing were performed from August 2023 to March 2024; neither paper gives a date for any individual test.
  7. LR-0007: Tested by what the paper calls a direct injection technique, under both pharmacopoeias. The paper reports the lyophilised powder free of viable microorganisms at the time of testing; it does not test the vial after reconstitution or storage. Named under the sample-control rule: the study team bought this product itself, and the paper reports its results separately from the other products. Test date: The research letter on this study states that test purchases and analytical testing were performed from August 2023 to March 2024; neither paper gives a date for any individual test.
  8. LR-0008: Endotoxin measured at 8.9511 EU/mg by kinetic turbidimetric assay (Ph. Eur. 2.6.14, USP <85>), the highest of the three; the paper says it indicates potential environmental contamination during production. No limit is stated, so no pass or fail is given here. Named under the sample-control rule: the study team bought this product itself, and the paper reports its results separately from the other products. Test date: The research letter on this study states that test purchases and analytical testing were performed from August 2023 to March 2024; neither paper gives a date for any individual test.
  9. LR-0009: Measured 1.34 mg (SD 0.07) against 1 mg on the label: 33.58% more than labelled, which is the paper's own labelling-accuracy figure. The same method read the genuine Ozempic 1 mg pen at +5.05% over its label. A reader dosing by the label would receive more than intended. Named under the sample-control rule: the study team bought this product itself, and the paper reports its results separately from the other products. Test date: The research letter on this study states that test purchases and analytical testing were performed from August 2023 to March 2024; neither paper gives a date for any individual test.
  10. LR-0010: The paper's purity is semaglutide as a share of the whole powder in the vial (1.34 mg of 14.9 mg), not the chromatographic peptide purity a research-grade '99%' claim usually means; the paper found no peptide-like impurities. So the vial is mostly undeclared non-peptide material, and the two percentages measure different things. The measurement stands; the comparison is not like-for-like. Named under the sample-control rule: the study team bought this product itself, and the paper reports its results separately from the other products. Test date: The research letter on this study states that test purchases and analytical testing were performed from August 2023 to March 2024; neither paper gives a date for any individual test.
  11. LR-0011: Tested by what the paper calls a direct injection technique, under both pharmacopoeias. The paper reports the lyophilised powder free of viable microorganisms at the time of testing; it does not test the vial after reconstitution or storage. Named under the sample-control rule: the study team bought this product itself, and the paper reports its results separately from the other products. Test date: The research letter on this study states that test purchases and analytical testing were performed from August 2023 to March 2024; neither paper gives a date for any individual test.
  12. LR-0012: Reported as below 2.8658 EU/mg by kinetic turbidimetric assay (Ph. Eur. 2.6.14, USP <85>) — an upper bound, not a measured level, although the paper's abstract describes endotoxin as detected in all samples. No limit is stated, so no pass or fail is given here. Named under the sample-control rule: the study team bought this product itself, and the paper reports its results separately from the other products. Test date: The research letter on this study states that test purchases and analytical testing were performed from August 2023 to March 2024; neither paper gives a date for any individual test.

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Studies we screened that do not meet the rules yet. They are listed so that leaving them out is visible, not silent.

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