Independent · non-commercial · publishes on a quarterly cycle|Current cycle 2026 Q3
Compound Evidence InstituteEvidence synthesis · established 2023Graded assessments of compounds, trials, methods and supply
Document set current to 30 July 2026
Supplier dossier · §3

QST — third-party testing record

The third-party reports the Institute examined, what each determined, and the provenance of each sample.

Document identifier
CEI-SD-19/3
Series
Supplier dossier
Version
2.0
Published
29 Aug 2026
Last reviewed
29 Aug 2026
Next review
29 Aug 2027
Identifier
10.71829/cei.supp.19
Certainty
Not rated
Cycle
2026 Q3
Assessment score
60.0 / 100
Conformance
C

The Institute assesses documentation, not product. It has purchased nothing, tested nothing and inspected nothing. Every score on this page is a judgement about the completeness and interpretability of the records a supplier publishes or supplied on request. A high score means that a supplier documents its material well. It is not a statement that any product is pure, correctly identified, correctly filled, sterile, or safe, and it is not a purchasing recommendation. The Institute makes no purchasing recommendations.

§3Third-party testing record

The Institute records the third-party reports it has been able to obtain for this supplier, what each determined, and what each left undetermined. It has commissioned none of these reports and has not verified that the material tested is representative of the material supplied. Where a report was supplied by the supplier rather than obtained independently, the sample was chosen by the party being assessed, which is recorded at §3.2.

§3.1Reports examined

Table 1. Third-party analytical reports examined for QST, with the determinations each carried. Empty cells record a determination that was not made or not reported, not a failure.

Report dateCompoundPurity, % areaIdentity methodContentWaterCounter-ionBatch link
24 Jun 2026Teduglutide97.82ESI-MS, nominal mass onlyTraceable
22 Jun 2026Tirzepatide96.47ESI-MS, nominal mass onlyTraceable
27 Feb 2026Larazotide acetate98.16ESI-MS, nominal mass onlyTraceable
23 Feb 2026GHRP-699.53ESI-MS, nominal mass onlyTraceable
19 Feb 2026Thymosin beta-499.80ESI-MS, nominal mass onlyTraceable
25 Jan 2026AOD-960498.66ESI-MS, nominal mass onlyTraceable
06 Dec 2025Semaglutide, oral99.80ESI-MS, nominal mass onlyTraceable
10 Nov 2025Liraglutide95.80ESI-MS, nominal mass onlyTraceable
06 Nov 2025Hexarelin96.40ESI-MS, nominal mass onlyTraceable
05 Oct 2025Retatrutide99.16ESI-MS, nominal mass onlyTraceable
21 Sep 2025Liraglutide99.35ESI-MS, nominal mass onlyTraceable
09 Aug 2025TB-50098.68ESI-MS, nominal mass onlyTraceable
19 Jun 2025Exenatide95.44ESI-MS, nominal mass onlyTraceable
11 May 2025Semaglutide99.57ESI-MS, nominal mass onlyTraceable
28 Apr 2025IGF-1 LR399.65ESI-MS, nominal mass onlyTraceable
11 Apr 2025Retatrutide99.46ESI-MS, nominal mass onlyTraceable
31 Jan 2025BPC-15798.65ESI-MS, nominal mass onlyTraceable
25 Jan 2025GHRP-299.80ESI-MS, nominal mass onlyTraceable
20 Dec 2024Dulaglutide98.93ESI-MS, nominal mass onlyTraceable
19 reports examined. A purity figure without a named method indicates that chromatography was performed and little more; 19 of these reports carry no content determination and therefore do not permit a mass balance to be formed.
Trend
Figure 2. Reported purity across the examined reports, in date order. The figure conveys dispersion and nothing more: these are area percentages obtained under methods that differ between reports, and comparing them to two decimal places would attribute a precision to the series that it does not have.

§3.2Provenance of the tested samples

Table 2. Provenance of the samples underlying the reports above. Sample provenance determines what a report can support.

ProvenanceReportsWhat it supports
Supplier-selected14The supplier chose which material to submit. A favourable result establishes that the supplier can produce material of that quality, and not that a given order will be of that quality.
Independently purchased3The stronger class of evidence. Establishes what an ordinary purchaser received on one occasion.
Provenance not recorded2Cannot be placed in either class, and the Institute treats it as the weaker.
Provenance counts are the Institute’s classification of the reports it examined and are not published figures of any supplier.

References cited on this page

References are numbered in order of first citation in this document. Each superscript in the text links to its entry below.

  1. Sodhi M, Rezaeianzadeh R, Kezouh A, Etminan M. Risk of gastrointestinal adverse events associated with glucagon-like peptide-1 receptor agonists for weight loss. JAMA 2023;330(18):1795–1797. doi:10.1001/jama.2023.19574 · PMID 37796527
  2. United States Pharmacopeial Convention. General Chapter ⟨1225⟩ Validation of Compendial Procedures. United States Pharmacopeia — National Formulary (USP–NF) 2024;USP 2024 Issue 1. identifier not held by the Institute

Identifiers are reproduced only where the Institute holds them. Where a digital object identifier or PubMed identifier is not shown, the Institute has recorded the journal and year and has not constructed an identifier.

Nothing published by the Institute is medical advice, a diagnosis, a prescription, a treatment recommendation or a purchasing recommendation. Compounds supplied for research use are not approved for human or veterinary use in any jurisdiction, and a favourable analytical assessment of a supplier is not a statement that any product is safe or effective. The Institute publishes certainty ratings and never recommendations. No telephone number, messaging handle or ordering channel appears anywhere on this site.