Audit: QRS - Ipamorelin for Health & Longevity

Audit conducted on 07/08/2026 13:21 using AI4L / Opus 5

Iterations

Summary

Items Count
Total 91
Passed 81
Failed 0
N/A 10
Pass Rate 100.00%
  • Total = Passed + Failed + N/A
  • Pass Rate = Passed / (Passed + Failed) × 100
  • N/A items are excluded from the pass rate calculation

1. General Rules

# Description Result Comments
1.1 Every claim, magnitude, label, recommendation, and statement in the QRS is literally supported by content in the source ER. 🟢 All protocol, benefit, risk, contraindication, interaction, monitoring and qualitative content traces to ER lines 340–513 and 394–465.
1.2 Where the ER uses cautious phrasing (“not formally studied”, “None documented in human trials to date”, “theoretical concern”, “data are limited”), the QRS uses the same phrasing. 🟢 “Not validated in any human trial” (action_1_sub) mirrors ER line 396; “no controlled data confirm this for ipamorelin” (time_2_sub) is verbatim from ER line 459; “Theoretical promotion of occult neoplasia” retains the ER hedge.
1.3 The QRS never strengthens an ER claim (e.g., “not formally studied” → “not required”) or softens one (e.g., “do not use during pregnancy” → “use with caution during pregnancy”). 🟢 Contraindications remain absolute; interactions remain cautions; no tier or hedge was upgraded or downgraded.
1.4 The QRS does not relabel an ER fact under a different decision category. A “Benefit-Modifying Factor” from ER section is not surfaced as a “Caution”; a “Risk-Modifying Factor” is not surfaced as a “Side Effect”; etc. 🟢 Gates draw only from ER Key Interactions & Contraindications; Benefits/Risks draw only from the respective ER tiered sections; no Benefit- or Risk-Modifying Factor was migrated.
1.5 PubMed IDs, study citations, expert names, clinical trial identifiers (NCT*), and brand names appear in the QRS only if they appear in the source ER for the same fact. 🟢 No PMIDs, NCT IDs or expert names appear; every named drug (insulin glargine, glipizide, octreotide, semaglutide, etc.) is present in the corresponding ER interaction bullet.
1.6 The QRS does not introduce new attributions. 🟢 No attributions of any kind are present in the QRS.

2. Focus, Tone & Audience

# Description Result Comments
2.1 The QRS follows the tone of the ER, which is determined by the ER’s own language, phrasing, and framing. 🟢 Sober, evidence-graded register matching the ER throughout.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Targets and cadence give actionable structure; evidence gaps are stated without alarm.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 Content is descriptive (“most commonly quoted”, “least favoured”), not directive.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 No imperatives; monitoring targets are stated as ranges carried verbatim from the ER table.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No occurrence of “recommend”, “advise”, “should” in the document’s own voice.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person pronouns anywhere in the QRS.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Technical terms are expanded (rapid eye movement sleep, apnea-hypopnea index, growth hormone) rather than left as acronyms.
2.8 Information is presented in a concise and very compact manner 🟢 Gate, benefit and risk items are noun phrases; ER mechanistic tails are stripped throughout.
2.9 It DOES NOT address the reader directly 🟢 Confirmed: no “you”, “your”, or imperative constructions.
2.10 The target audience is health- and longevity-oriented adults who are risk-aware, proactive, and actively seeking to optimize health or apply the intervention under review. 🟢 14-marker panel, cycling blocks and identity-verification framing address a proactive optimizer.
2.11 The target audience is willing to employ lifestyle and behavioral changes as well as follow protocols that may be inconvenient, costly, or require effort. 🟢 Fasted bedtime dosing, DXA, continuous laboratory surveillance and injection-site rotation are presented without qualification about effort.
2.12 The document is NOT written for the general population, who are unwilling to employ lifestyle and behavioral changes or follow protocols that may be inconvenient, costly, or require effort. 🟢 No simplification toward general-population framing.
2.13 Framing, takeaways, and risk/benefit weighting throughout the document reflect this audience, including where an intervention’s signal for the average person differs from its signal for this audience. 🟢 At-a-glance leads with the evidence vacuum and supply problem, which are the decision-relevant points for this audience.
2.14 The document’s own voice frames usage in longevity terms, not “anti-aging” (e.g., “anti-aging clinics”, “anti-aging community”, “anti-aging medicine”). Proper names that contain “anti-aging” (e.g., “American Academy of Anti-Aging Medicine”) are quoted verbatim. 🟢 The string “anti-aging” does not occur in the QRS; the header uses “Health & Longevity”.
2.15 The document’s own voice uses formal clinical and scientific terminology, not colloquial or consumer-grade language (e.g., “oral medication” not “pill(s)”; “injection” not “shot”; “adverse event” not “bad reaction”). Direct quotes from sources are exempt. 🟢 “subcutaneously”, “adverse effects”, “injection sites”, “gray-market” — all consistent with the ER’s own register.

3. Template Integrity

# Description Result Comments
3.1 The following labels and headings on the QRS are fixed and not modified: Card and section headings: “Protocol”, “Time to effect”, “Benefits”, “Risk & Side Effects”, “Monitoring”, “Qualitative Assessment”; Gate headings: “Contraindications”, “Key Interactions”; Tier labels: “High”, “Medium”, “Low”, “Speculative”; Table column headers in Monitoring: “Marker”, “Target”, “Why” 🟢 All sixteen fixed strings verified byte-for-byte against the template at lines 440, 477, 519, 539, 557, 582, 601, 605–607, 775 and the tier labels in Benefits and Risks.
3.2 All “” from the [qrs_template] are present in the the QRS. 🟢 All 37 template variable names present; marker_#_* expanded to markers 1–14 and qualitative_item_# to items 1–8.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 Structural diff against the template shows changes only inside data-qrs-var spans; website="evidence_review", website="audit" and website="full_review" spans are untouched.

4. Formatting

# Description Result Comments
4.1 When the source ER section is empty, the QRS uses the ER’s own empty-state phrasing verbatim. Typical phrasings are “None documented in human trials to date” and “Not formally studied” N/A No ER section feeding the QRS is empty; all four benefit tiers, all four risk tiers, both gates, Monitoring and Qualitative are populated.
4.2 Where the ER presents a bulleted item as “Label: content”, the QRS uses the ER’s bold label verbatim as the cell or row label. 🟢 Protocol labels “Standard clinic protocol”, “Best time of day”, “Single versus split dosing” and all eight qualitative labels match the ER bold labels verbatim (ER lines 398, 410, 414, 504–511).
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 No label deviates from its ER source; monitoring marker names match the ER biomarker table column 1 exactly.
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). Color and emphasis are conveyed through CSS and bold labels. 🟢 Unicode scan of the file returns no emoji code points; the ER’s ⚠️ Conflicted markers were correctly stripped.
4.5 The QRS is designed to render on one A4 page. Any section that has more content in the ER than fits the per-section budget is condensed by the LLM, not extended onto a second page. 🟢 Every section is condensed to its minimum form — gate and tier items are bare noun phrases, monitoring “why” strings are single clauses, qualitative items drop the ER’s rationale tails.

5. Metadata

# Description Result Comments
5.1 The metadata is placed inside a single HTML comment that is the first element after “<!doctype html>” and before any other comment, head, or body content. 🟢 Comment opens at line 2, immediately after the doctype at line 1, and closes at line 14.
5.2 Inside that HTML comment the YAML block is delimited by a line “—” opening and a line “—” closing. Text before the opening “—” is permitted but is not parsed as YAML. 🟢 Opening --- at line 3, closing --- at line 13; the descriptive text on line 2 precedes the block.
5.3 The metadata is not visible in any rendered view of the QRS and is not surfaced by any other element on the sheet. 🟢 Enclosed in an HTML comment; no metadata value is duplicated in visible markup.
5.4 All frontmatter values are trimmed: no leading or trailing whitespace, no surrounding quotes unless the value contains a colon, bracket, or leading special character that requires YAML quoting. 🟢 Only duration: "00:03" is quoted, correctly, because it contains a colon.
5.5 The filename of the source ER is stated as “er_filename: [er_filename]” 🟢 Line 4: er_filename: ipamorelin_2026-0807-0553_Opus_ER.md.
5.6 Version of the QRS.md file used to create the document is stated as “qrs_prompt_version: [Version of QRS.md]” 🟢 Line 5: qrs_prompt_version: 26.7.02, matching the QRS.md version badge.
5.7 Creation date and time of the document is stated as “qrs_creation_date: [YYYY-MMDD-HHMM]” (e.g., 2026-0501-1430) 🟢 Line 6: qrs_creation_date: 2026-0807-1307.
5.8 The nickname of the AI used to create the document is stated as “qrs_creator_ai_nickname: [qrs_creator_ai_nickname]” 🟢 Line 7: qrs_creator_ai_nickname: Opus.
5.9 The nickname of the AI is just a single word model name without version, etc. (e.g., Opus, Sonnet, Grok, Gemini, ChatGPT) 🟢 “Opus” — single word, no version.
5.10 The full name of the AI used to create the document is stated as “qrs_creator_ai_fullname: [qrs_creator_ai_fullname]” 🟢 Line 8: qrs_creator_ai_fullname: Opus 5.
5.11 The full name of the AI consists of the [qrs_creator_ai_nickname] and the model version number and no additional qualifier (e.g., Opus 4.6, Sonnet 3.2, Grok 4.5, Gemini 3.1, ChatGPT 5.4) 🟢 “Opus 5” — nickname plus version, no qualifier.
5.12 The filename of the document is stated as “qrs_filename: [filename of this document]” 🟢 Line 9: qrs_filename: ipamorelin_2026-0807-0553_Opus_QRS.html, matching the file on disk.
5.13 All frontmatter values are trimmed: no leading or trailing whitespace, no surrounding quotes unless the value contains a colon, bracket, or leading special character that requires YAML quoting. 🟢 Re-verified across all nine keys; no stray whitespace or unnecessary quoting.

6. Page Title & Header

# Description Result Comments
6.1 [page_title] is set to the [canonical_topic] of the ER frontmatter followed by “ - Quick Reference Sheet” (e.g., “Intervention - Quick Reference Sheet”). The [canonical_topic] is HTML-entity-encoded as needed (e.g., &amp; for &) 🟢 Line 22: Ipamorelin for Health &amp; Longevity - Quick Reference Sheet, matching ER canonical_topic with the ampersand encoded.
6.2 [header_topic] is set to the [canonical_topic] of the ER frontmatter, with HTML entities encoded as needed (e.g., &amp; for &) 🟢 Line 417: Ipamorelin for Health &amp; Longevity.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 Line 421: 08/07/2026, correctly derived from 2026-0807-1307.
6.4 [header_subline_model] is set to [qrs_creator_ai_fullname] 🟢 Line 425: Opus 5.
6.5 No additional header content appears: no badge, version stamp, AKA / alternate names line, source-AI attribution, audit date, or QRS variant marker. 🟢 Header contains only title and the template’s fixed subline; the ER’s “Also known as” line was not carried over.

7. At-A-Glance Section

# Description Result Comments
7.1 [at_a_glance] is dense, execution-oriented summary of the ER Conclusion section 🟢 Condenses ER line 535: mechanism, selectivity claim, halted human programme, absent outcome data, supply and anti-doping status.
7.2 [at_a_glance] is no longer than 60 words 🟢 Exactly 60 words.
7.3 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 Five-amino-acid peptide, absent stress-hormone rise, halted human study, unmeasured outcomes, no lawful US supply, substituted gray-market material and sport ban all map to distinct clauses of ER line 535.
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 No acronyms; “growth hormone”, “stress-hormone”, “gray-market material” and “molecule” are all plain-language.
7.5 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial name, year, n or p-value appears.
7.6 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 No numeric effect estimate appears.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All eleven items come from the “Populations who should avoid this intervention” bullet at ER line 368.
8.2 [stop_items] represent the Contraindications from the ER 🟢 All eleven ER contraindications are present, none added.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Lines 542–552: eleven <li> elements inside the stop_items span.
8.4 Items are as concise as possible. No trailing explanations, no elaborations, no mechanistic rationale, no attributions, no citations, no study details. No content after an em-dash, en-dash, or hyphen-dash (e.g., “— dose reduction required”, “— reduced efficacy”) — these trailing clauses are stripped. Just the key fact. 🟢 The ER’s trailing rationales (“where high-dose growth hormone approximately doubled mortality”, “where sodium and water retention is poorly tolerated”) are stripped; no dashes remain.
8.5 Parenthetical qualifiers from the ER bullet — time windows, severity classes, threshold values, clinical staging — ARE preserved as part of the item, kept as concise as possible (shortened or trimmed where needed to fit the one-page budget, but never dropped entirely). 🟢 “within the past 5 years”, “HbA1c above 8.0%”, “apnea-hypopnea index of 30 or greater”, “Class III or IV”, “stage 4 or 5” and “open epiphyseal growth plates” all retained.
8.6 When the ER uses ranking notation inside parens (e.g., “>” for severity ordering) that depends on an explanatory phrase to interpret, normalize the items to a plain comma-separated list rather than carrying through the bare symbol. N/A The ER contraindication bullet uses no ranking notation inside parentheses.
8.7 If no [stop_items] are present the section is left empty N/A Eleven stop_items are present.

9. Key Interactions

# Description Result Comments
9.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All thirteen items map to the thirteen interaction bullets at ER lines 342–366.
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 Thirteen of thirteen ER interaction bullets carried over; no overlap with the eleven contraindications.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Lines 560–572: thirteen <li> elements inside the caution_items span.
9.4 Items are as concise as possible. No trailing explanations, no elaborations, no mechanistic rationale, no attributions, no citations, no study details. No content after an em-dash, en-dash, or hyphen-dash (e.g., “— dose reduction required”, “— reduced efficacy”) — these trailing clauses are stripped. Just the key fact. 🟢 Every ER caution class, mechanism sentence and “Mitigation:” clause is stripped; the ER’s “Other interventions — “ dash prefix is removed.
9.5 Parenthetical qualifiers from the ER bullet — example drug lists, time windows, severity classes, threshold values, clinical staging — ARE preserved as part of the item, kept as concise as possible (shortened or trimmed where needed to fit the one-page budget, but never dropped entirely). 🟢 All named example drugs are retained in every bullet; only the supplement dose amounts are trimmed, with the agent names kept. The niacin threshold “500 mg and above” is preserved.
9.6 When the ER uses ranking notation inside parens (e.g., “>” for severity ordering) that depends on an explanatory phrase to interpret, normalize the items to a plain comma-separated list rather than carrying through the bare symbol. N/A The ER interaction bullets use no ranking notation inside parentheses.
9.7 If no [caution_items] are present the section is left empty N/A Thirteen caution_items are present.

10. Protocol

# Description Result Comments
10.1 The section is derived from the ER Protocol section 🟢 All three cells derive from ER Therapeutic Protocol lines 396–414.
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 Dose/route/cycle length, timing, and dosing frequency — the three decisions a user must make before the first injection.
10.3 If less that three distinct actionable implementation aspects are mentioned in the ER the unused sets are left empty and made invisible, not filled with placeholder text or empty-state phrasing. N/A The ER supplies more than three actionable aspects; all three sets are used.
10.4 All used [action_#label], [action#value], [action#_sub] items are filled with meaningful content derived from the ER Protocol section. 🟢 Nine of nine action variables populated; the “Not validated in any human trial” caveat carries ER line 396 forward.

11. Time to Effect

# Description Result Comments
11.1 The three sets of [time] items cover the three most important time-to-effect aspects from the ER 🟢 Growth hormone pulse, sleep depth and body composition, from the ER “Time to effect” bullet at line 459; the IGF-1 window is folded into time_3_sub.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Ordered High tier (acute growth hormone release) then Low tier (sleep, fat-free mass), matching the ER benefit grading.
11.3 If less that three distinct time-to-effect aspects are mentioned in the ER the unused sets are left empty and made invisible, not filled with placeholder text or empty-state phrasing. N/A The ER supplies four time-to-effect aspects; all three sets are used.
11.4 All used [time_#label], [time#value], [time#_sub] items are filled with meaningful content derived from the ER. 🟢 Nine of nine time variables populated with ER-sourced content.
11.5 If the ER does not provide any information on time to effect, the section is removed completely from the Protocol Panel N/A The ER provides time-to-effect information at line 459.

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 All thirteen items map to the ER benefit headings at lines 148–216.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four spans present and populated at lines 521–532.
12.3 Items are as concise as possible. No explanations, no elaborations, no effect sizes, no qualifiers, no attributions, no citations, no study details, no mechanistic explanations, etc. Just the key fact. 🟢 Mechanistic tails dropped (“Through Sustained Growth Hormone Axis Stimulation”); no magnitudes, PMIDs or study details carried over.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses appear in any benefits span.
12.5 If no items of a specific sub-section (high, medium, low, speculative) are present the respective is set to “display=none”, not filled with “None documented in human trials to date” or similar empty-state phrasing. N/A All four benefit tiers contain items in the ER.

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 All thirteen items map to the ER risk headings at lines 242–320.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four spans present and populated at lines 584–595.
13.3 Items are as concise as possible. No explanations, no elaborations, no effect sizes, no qualifiers, no attributions, no citations, no study details, no mechanistic explanations, etc. Just the key fact. 🟢 Mechanistic tails dropped (“via IGF-1”, “Through Sustained Growth Hormone and IGF-1 Signalling”); no magnitudes or citations carried over.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses appear in any risks span.
13.5 If no items of a specific sub-section (high, medium, low, speculative) are present the respective is set to “display=none”, not filled with “None documented in human trials to date” or similar empty-state phrasing. N/A All four risk tiers contain items in the ER.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 Rows derive from the ER biomarker table at lines 485–500.
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All fourteen ER biomarkers present in ER order, with target strings carried verbatim.
14.3 [monitoring_cadence] is populated with the monitoring cadence/frequency derived from the ER Monitoring section. It is not left with placeholder text or empty. 🟢 Line 769 reproduces the baseline window, the 4-week / 12-week / 3–6-month cadence and the dose-escalation reset from ER lines 481–483.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 All eight items come from the qualitative marker list at ER lines 504–511.
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 Eight of eight ER qualitative markers present, with the ER bold labels verbatim and rationale tails stripped.

Issues 07/08/2026 13:21

Pass rate 100.00%. No issues found.

Issues 07/08/2026 13:15

  1. 1.1 / 1.3 / 7.3 — Unqualified “no lawful supply” claim: [at_a_glance] (line 433) states “No lawful supply exists in the United States”, dropping the ER’s qualifier; the ER says “no lawful pharmaceutical supply exists in the United States” (Conclusion, line 535) and separately notes that personal-use possession or importation “occupies an enforcement gray zone” (line 463), so the unqualified form strengthens the claim beyond its source.

Fixes 07/08/2026 13:15

  1. 1.1 / 1.3 / 7.3 — Unqualified “no lawful supply” claim: [at_a_glance] now reads “No lawful pharmaceutical supply exists in the United States”, restoring the ER’s qualifier; “or lifespan effects” was trimmed to “or lifespan” to keep the section at the 60-word limit.