Audit: QRS - Cannabidiol for Health & Longevity

Audit conducted on 22/09/2026 16:45 using AI4L / Opus 5

Iterations

Summary

Items Count
Total 94
Passed 84
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 doses (15–50 mg, 150–300 mg), timings (2.5 weeks, 60–90 minutes, 2–4 weeks), thresholds (3× ULN, 2× ULN) and biomarker ranges trace to ER lines 397–419, 452, 480–492.
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. 🟢 hs-CRP row retains “which is unproven in humans”; time_3_sub retains “Where present, in the trials that found them”.
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”). 🟢 Avoid-list populations stay in Contraindications; transplant immunosuppressants remain an absolute gate rather than a caution.
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. 🟢 Every card draws from its own ER section; no Benefit- or Risk-Modifying Factor is surfaced as a gate.
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, citations, author names, NCT identifiers or brand names anywhere in the QRS.
1.6 The QRS does not introduce new attributions. 🟢 No attributions present.

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-bounded register matching the ER Conclusion.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 States what is established, what conflicts, and what to measure, without hedging or alarm.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 No imperatives; protocol cells describe observed practice (“Split twice-daily dosing was used in every pivotal trial”).
2.4 The QRS avoids language that implies medical or clinical advice 🟢 Descriptive throughout; only the template disclaimer addresses clinical decisions.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 Cadence and protocol cells are stated as noun phrases, not recommendations.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person pronouns present in the file.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Technical terms are confined to the Monitoring table and interaction gates where they are decision-bearing; ALT/AST are expanded in the table.
2.8 Information is presented in a concise and very compact manner 🟢 All list items are key-fact fragments with no explanatory tails.
2.9 It DOES NOT address the reader directly 🟢 Confirmed: no “you”/”your” anywhere.
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. 🟢 Nine-marker monitoring panel and batch-verification gate assume a proactive, risk-aware reader.
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. 🟢 Cadence requires repeated liver panels and daily home blood pressure.
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. 🟢 Content assumes access to laboratory testing and drug-level monitoring.
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. 🟢 The lede foregrounds the consumer-dose translation gap; qualitative_item_4 frames appetite loss as unwanted “at this stage of life”.
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. 🟢 No occurrence of “anti-aging” in the QRS.
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)”; “oral” / “administered orally” not “taken by mouth” / “given by mouth”; “injection” not “shot”; “adverse event” not “bad reaction”). This holds on EVERY surface, including the QRS lede — the stricter plain-language bar (see 2.7) does not license lay phrasing for route of administration. Direct quotes from sources are exempt. 🟢 Route of administration is given as “oral dose” / “Oil or softgel”; dosage forms named formally; no colloquial substitutes.

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 fixed headings, gate headings, tier labels and table headers match the template byte-for-byte.
3.2 All “…” from the [qrs_template] are present in the the QRS. 🟢 All 34 named template spans present; the repeating marker_#/qualitative_item_# spans are instantiated as marker_1–9 and qualitative_item_1–6.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 Stylesheet, structure, website=”evidence_review”/”audit”/”full_review” spans and footer disclaimer are identical to the template.

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 source ER section that feeds the QRS is empty.
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. 🟢 “Consumer oral protocol”, “Best time of day”, “Baseline biomarkers” and the interaction labels reproduce the ER bold labels; Monitoring row names match the ER biomarker column.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 Time-to-effect labels are drawn from the ER’s own wording in Practical Considerations (“Acute calming”, “Blood-pressure reductions”, “Sleep and pain effects”).
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). Color and emphasis are conveyed through CSS and bold labels. 🟢 No emoji present; the ER’s “⚠️ Conflicted” markers were correctly dropped.
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 reduced to key-fact fragments; no explanatory prose, effect sizes or citations were carried over.

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. 🟢 Lines 2–14, immediately after <!doctype html> on line 1.
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.
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 repeated in the body.
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: "00:02" is quoted, correctly, because it contains a colon.
5.5 The filename of the source ER is stated as “er_filename: [er_filename]” 🟢 er_filename: cannabidiol_2026-0907-0235_Opus_ER.md at line 4.
5.6 Version of the QRS.md file used to create the document is stated as “qrs_prompt_version: [Version of QRS.md]” 🟢 qrs_prompt_version: 26.9.22, matching QRS.md.
5.7 Creation date and time of the document is stated as “qrs_creation_date: [YYYY-MMDD-HHMM]” (e.g., 2026-0501-1430) 🟢 qrs_creation_date: 2026-0922-1625.
5.8 The nickname of the AI used to create the document is stated as “qrs_creator_ai_nickname: [qrs_creator_ai_nickname]” 🟢 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) 🟢 Single word “Opus”.
5.10 The full name of the AI used to create the document is stated as “qrs_creator_ai_fullname: [qrs_creator_ai_fullname]” 🟢 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” carries no trailing qualifier.
5.12 The filename of the document is stated as “qrs_filename: [filename of this document]” 🟢 qrs_filename: cannabidiol_2026-0907-0235_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. 🟢 Confirmed across all nine keys.

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 &) 🟢 “Cannabidiol for Health & Longevity - Quick Reference Sheet” at line 22.
6.2 [header_topic] is set to the [canonical_topic] of the ER frontmatter, with HTML entities encoded as needed (e.g., &amp; for &) 🟢 “Cannabidiol for Health & Longevity” at line 417.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 2026-0922 rendered as 09/22/2026.
6.4 [header_subline_model] is set to [qrs_creator_ai_fullname] 🟢 “Opus 5” at line 425.
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 matches the template exactly; the ER’s alternate-names line was not carried over.

7. At-A-Glance Section

# Description Result Comments
7.1 [at_a_glance] opens by saying what the intervention is — its kind (e.g., dietary supplement, prescription medication, peptide, plant, procedure, practice) — and what it is used for, in plain language, before any verdict on the evidence 🟢 Opens “Cannabidiol is the non-intoxicating fraction of cannabis, sold as oils, capsules and creams for sleep, pain and stress” before any evidence verdict.
7.2 [at_a_glance] is dense, execution-oriented summary of the ER Conclusion section 🟢 Compresses the Conclusion’s two established effects, the conflicted claims and the dominant harms.
7.3 [at_a_glance] is no longer than 70 words 🟢 69 words.
7.4 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 Product forms and use cases from ER line 37; the two established effects, conflicted claims and harms from ER lines 525–527.
7.5 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 No acronyms; “around-the-clock blood pressure” replaces “24-hour ambulatory”, “raised blood levels of other medicines” replaces the interaction terminology.
7.6 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial names, years or sample sizes.
7.7 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 No mmHg figures, odds ratios or confidence intervals.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 Sourced from the “Populations who should avoid Cannabidiol” list at ER lines 369–375.
8.2 [stop_items] represent the Contraindications from the ER 🟢 All seven avoid-list populations are present, plus the transplant-immunosuppressant absolute contraindication from ER line 349.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Seven <li> elements inside the 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 rationale tail “on the absence of human safety data rather than demonstrated harm” and the Child-Pugh gloss were stripped; no dash-led clauses 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). 🟢 “three times the upper limit of normal”, “twice the upper limit of normal”, “Child-Pugh Class B or C” and “without transplant-clinic supervision” 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 uses no ranking notation in this section.
8.7 The section is left empty ONLY IF the ER’s Key Interactions & Contraindications section identifies no population, condition, or scenario for which the intervention should be avoided, deferred, or used only under specialist supervision. 🟢 The ER identifies such populations and the section is correctly populated.
8.8 If the section is left empty, an HTML comment inside the [stop_items] span records the ER basis for the absence, naming or quoting the ER text relied on. E.g. N/A The section is not empty.

9. Key Interactions

# Description Result Comments
9.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All eleven items map to ER bullets at lines 343–365.
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 Eleven of the ER’s twelve interaction bullets; transplant immunosuppressants correctly excluded because they sit in Contraindications.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Eleven <li> elements inside the 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. 🟢 Severity words, consequences and mitigation sentences were all stripped; no dash-led clauses remain.
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). 🟢 Every named example drug list is preserved verbatim; only the purely definitional glosses (“CYP2C9 clears many drugs”, “CYP1A2 clears caffeine and several drugs”) were dropped as elaborations under 9.4.
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 uses no ranking notation in this section.
9.7 The section is left empty ONLY IF the ER’s Key Interactions & Contraindications section identifies no interaction, additive effect, or exposure that changes how the intervention is used. 🟢 The ER identifies twelve such interactions and the section is correctly populated.
9.8 If the section is left empty, an HTML comment inside the [caution_items] span records the ER basis for the absence, naming or quoting the ER text relied on. E.g. N/A The section is not empty.

10. Protocol

# Description Result Comments
10.1 The section is derived from the ER Protocol section 🟢 All three cells map to bullets in the ER Therapeutic Protocol section (lines 397, 411, 419).
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 Dose, timing and pre-start safety testing — the three decisions a reader must make before and at first use.
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 provides 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. 🟢 All nine fields carry ER-derived content; no placeholders remain.

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 🟢 Exactly the three aspects named in the ER’s “Time to effect” bullet at line 452.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Blood pressure (High-tier benefit) leads, ahead of the two Low-tier benefits.
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 Three distinct aspects exist and 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. 🟢 All nine fields populated; time_1_sub also carries the steady-state note from ER line 409.
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, so the section is correctly retained.

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 Every item corresponds to an ER Expected Benefits subheading.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four spans present and populated.
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. 🟢 Items are the ER subheadings alone; no Magnitude paragraphs or mechanism text carried over.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parenthetical content in any benefits item.
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 tiers have 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 correspond to ER Potential Risks & Side Effects subheadings.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four spans present and populated.
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. 🟢 Frequencies, odds ratios and mechanistic notes were all dropped; “THC” expanded to plain “tetrahydrocannabinol” as the ER prose does.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parenthetical content in any risks item.
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 tiers have items in the ER.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 Rows reproduce the ER Monitoring Protocol & Defining Success biomarker table (lines 482–492).
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All nine ER biomarkers present, with optimal ranges and rationales matching the ER table.
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. 🟢 Baseline, 1/3/6-month and 6–12-month liver panel, blood-pressure and drug-level cadence taken from ER lines 480 and 492.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 Sourced from the qualitative-marker list at ER lines 496–501.
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All six qualitative markers present and unabridged.

Issues 22/09/2026 16:45

Pass rate 100.00%. No issues found.

Issues 22/09/2026 16:33

  1. 4.2 / 4.3 — Interaction label abbreviated: At line 599 the Key Interactions item reads “Sedating antihistamines (diphenhydramine, doxylamine) and alcohol”, abbreviating the ER’s bold label at ER line 357, “Over-the-counter sedating antihistamines (diphenhydramine, doxylamine) and alcohol:”; the dropped “Over-the-counter” narrows which antihistamines the interaction applies to.

Fixes 22/09/2026 16:33

  1. 4.2 / 4.3 — Interaction label restored verbatim: Changed the Key Interactions item from “Sedating antihistamines (diphenhydramine, doxylamine) and alcohol” to the ER’s bold label verbatim, “Over-the-counter sedating antihistamines (diphenhydramine, doxylamine) and alcohol”.

Issues 22/09/2026 16:30

  1. 4.2 / 4.3 — Protocol cell labels not ER-verbatim: action_1_label (line 451) reads “Consumer Oral Dose” where the source bullet is labelled “Consumer oral protocol:” (ER line 397), and action_2_label (line 465) reads “Timing”, which matches no ER bold label — the cell’s content comes from “Best time of day:” (ER line 407) and “Single versus split dosing:” (ER line 411).

Fixes 22/09/2026 16:30

  1. 4.2 / 4.3 — Protocol cell labels made ER-verbatim: action_1_label changed from “Consumer Oral Dose” to the ER bullet label “Consumer oral protocol”, action_2_label from the invented “Timing” to the ER bullet label “Best time of day”, and action_3_label from “Baseline Biomarkers” to the ER’s exact casing “Baseline biomarkers”.