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
Consultation record

Public comment periods — page 4

120 consultations carrying 1,332 signed submissions. Every submission has a declared interest, a secretariat response and a disposition.

Consultations

120 documents · page 4 of 6
  • CEI-CP-019ClosedEvidence synthesis20 Apr 2025 – 20 May 2025

    Consultation on the draft safety review of the rodent thyroid C-cell signal observed with glucagon-like peptide-1 receptor agonists and its relevance to humans. The review assesses the mechanistic evidence for a species difference in…

    16 submissions
  • CEI-CP-073ClosedCompound monograph18 Apr 2025 – 16 May 2025

    Consultation on the draft monograph for Selank, which the assessment committee released for public comment before ratification. The draft grades the compound's principal assessed outcome at low certainty and states the basis for that…

    8 submissions1 not accepted
  • CEI-CP-078ClosedCompound monograph12 Apr 2025 – 10 May 2025

    Consultation on the draft monograph for TB-500, which the assessment committee released for public comment before ratification. The draft grades the compound's principal assessed outcome at very low certainty and states the basis for that…

    8 submissions
  • CEI-CP-037ClosedGovernance document04 Feb 2025 – 05 Apr 2025

    Consultation on the print and archival format for Institute documents: what a printed copy must carry so that it remains checkable when detached from the site, and what an archival copy must preserve.

    18 submissions4 not accepted
  • CEI-CP-107ClosedEvidence synthesis05 Feb 2025 – 02 Apr 2025

    Consultation on the draft of this scoping review, which registers the question: What randomised human evidence exists for BPC-157 in any indication?

    4 submissions
  • CEI-CP-099ClosedEvidence synthesis01 Feb 2025 – 29 Mar 2025

    Consultation on the draft of this intervention review, which registers the question: In adults at elevated cardiovascular risk, what is the effect of a glucagon-like peptide-1 receptor agonist compared with placebo on major adverse…

    13 submissions1 not accepted
  • CEI-CP-118ClosedEvidence synthesis24 Jan 2025 – 25 Mar 2025

    Consultation on the draft of this intervention review, which registers the question: In adults with type 2 diabetes, does tirzepatide achieve greater glycaemic and weight effect than semaglutide?

    7 submissions1 not accepted
  • CEI-CP-029ClosedGovernance document07 Feb 2025 – 24 Mar 2025

    Consultation on the terms governing the Institute's calculators. The draft states that a calculator implements a published formula, that it holds no user data, and that its output is a computation and not clinical advice.

    18 submissions3 not accepted
  • CEI-CP-005ClosedCompound monograph03 Feb 2025 – 20 Mar 2025

    Consultation on the third version of the semaglutide monograph. The revision incorporates the cardiovascular outcome evidence from SELECT, reported in the New England Journal of Medicine in 2023, and the kidney outcome evidence from FLOW…

    14 submissions1 not accepted
  • CEI-CP-087ClosedMethodological standard14 Jan 2025 – 15 Mar 2025

    Consultation on the draft of CEI-MS-06, which specifies the performance a determination must achieve for microbiological quality and states what the resulting figure does not establish. The draft states performance rather than prescribing…

    13 submissions2 not accepted
  • CEI-CP-051ClosedCompound monograph10 Jan 2025 – 21 Feb 2025

    Consultation on the draft monograph for GHRP-2, which the assessment committee released for public comment before ratification. The draft grades the compound's principal assessed outcome at low certainty and states the basis for that…

    7 submissions
  • CEI-CP-100ClosedEvidence synthesis24 Jan 2025 – 21 Feb 2025

    Consultation on the draft of this safety review, which registers the question: What is the incidence of gastrointestinal adverse events and of discontinuation for adverse events with incretin receptor agonists compared with placebo?

    12 submissions2 not accepted
  • CEI-CP-046ClosedCompound monograph20 Jan 2025 – 17 Feb 2025

    Consultation on the draft monograph for Dulaglutide, which the assessment committee released for public comment before ratification. The draft grades the compound's principal assessed outcome at high certainty and states the basis for that…

    11 submissions
  • CEI-CP-050ClosedCompound monograph11 Jan 2025 – 08 Feb 2025

    Consultation on the draft monograph for GHK-Cu, which the assessment committee released for public comment before ratification. The draft grades the compound's principal assessed outcome at low certainty and states the basis for that…

    7 submissions1 not accepted
  • CEI-CP-102ClosedEvidence synthesis06 Nov 2024 – 01 Jan 2025

    Consultation on the draft of this intervention review, which registers the question: In adults with type 2 diabetes and chronic kidney disease, what is the effect of a glucagon-like peptide-1 receptor agonist on kidney outcomes?

    11 submissions
  • CEI-CP-028ClosedDocument series21 Oct 2024 – 20 Dec 2024

    Consultation on the structure of the document registry: the identifier scheme, the fields carried for every document, and the way a superseded document is represented. The draft assigns a permanent identifier at first publication and never…

    9 submissions1 not accepted
  • CEI-CP-115ClosedEvidence synthesis22 Oct 2024 – 17 Dec 2024

    Consultation on the draft of this safety review, which registers the question: Do incretin-based therapies increase the incidence of acute pancreatitis?

    10 submissions3 not accepted
  • CEI-CP-036ClosedMethodology02 Nov 2024 – 14 Dec 2024

    Consultation on the search-strategy template used across the synthesis series: the databases searched, the structure of the strategy, the handling of registry records without posted results, and the requirement that a strategy be published…

    19 submissions2 not accepted
  • CEI-CP-069ClosedCompound monograph14 Oct 2024 – 09 Dec 2024

    Consultation on the draft monograph for Semaglutide, oral, which the assessment committee released for public comment before ratification. The draft grades the compound's principal assessed outcome at high certainty and states the basis…

    9 submissions1 not accepted
  • CEI-CP-013ClosedGovernance document01 Nov 2024 – 01 Dec 2024

    Consultation on how the Institute should label a programme record it has constructed by grouping trials, as distinct from a programme as defined by its sponsor. The draft proposes a standing notice on every constructed record stating who…

    13 submissions3 not accepted

page 4 of 6

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.