Audit: QRS - Goji Berries for Health & Longevity

Audit conducted on 16/08/2026 16:31 using AI4L / Opus 5

Iterations

Summary

Items Count
Total 93
Passed 83
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 doses (15 g/day, 28 g/day five times weekly), time-to-effect values (28/45/90 days), benefit and risk labels, contraindications, interactions, biomarker targets, cadence and qualitative markers trace to ER lines 373–381, 430, 154–234, 258–306, 344–351, 326–342, 458–476.
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. 🟢 At-A-Glance keeps “supported but smaller” and “rest on weaker studies”; qualitative item 5 keeps “measured only in manufacturer-run trials”.
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 contraindications (line 563–571); interactions remain interactions (line 579–593). No tier or severity shift.
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. 🟢 Contraindications drawn only from the ER “Populations who should avoid Goji Berries” list; Key Interactions only from the ER interaction bullets. No Benefit- or Risk-Modifying Factor content appears.
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. 🟢 The QRS carries no PMIDs, citations, author names, NCT identifiers or brand names.
1.6 The QRS does not introduce new attributions. 🟢 No attributions of any kind 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. 🟢 Measured, sceptical register matching the ER (manufacturer-trial caveat, whole fruit over juice).
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Quantified targets and doses paired with plain-language framing.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 Content is stated as evidence and observed practice, not instruction.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 Cadence and qualitative items are reproduced from the ER’s own monitoring description rather than issued as advice.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No “recommend”, “advise” or “should” appears anywhere in the file.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person pronouns present.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Technical terms retained are the ER’s own bold labels and biomarker names, which items 4.2 and 14.2 require verbatim.
2.8 Information is presented in a concise and very compact manner 🟢 Benefits, Risks and gate items reduced to bare labels; no elaboration retained.
2.9 It DOES NOT address the reader directly 🟢 Confirmed; no direct address.
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 with functional ranges assumes a proactive, self-tracking audience.
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. 🟢 Retains the 28 g/day five-times-weekly macular schedule and macular pigment optical density testing.
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. 🟢 Specialist endpoints and tight functional ranges are well beyond 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. 🟢 Whole fruit over juice or extract, and the anticoagulant gate, are foregrounded as the decision-relevant distinctions.
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. 🟢 “anti-aging” does not appear; the title 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. 🟢 Formal terminology throughout; the plain-language wording in At-A-Glance is the ER’s own Conclusion phrasing and is required by item 7.4.

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 headings, gate labels, tier labels and column headers are byte-identical to the template (lines 446, 485, 527, 560, 576, 603, 628, 632–634, 760).
3.2 All “” from the [qrs_template] are present in the the QRS. 🟢 All 38 template variables present; marker_#* expanded to marker_1–9 and qualitative_item# expanded to items 1–5.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 Structural diff against the template shows changes only inside variable spans; the website=”evidence_review”, website=”audit” and website=”full_review” spans and all CSS 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 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. 🟢 “Standard whole-fruit protocol”, “Higher-dose macular protocol”, “Best time of day” and all nine interaction labels are carried verbatim from ER lines 373–381 and 326–342.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 Benefit and risk entries reuse the ER subsection headings; biomarker names reuse the ER table’s first column.
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 bare labels with no explanations; the A4 print block and @page rules from the template are intact (lines 377–391).

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 the doctype 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 header or 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: "00:03" 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: goji_berries_2026-0825-1311_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 badge version.
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: 2026-0816-1620.
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 matches the actual filename goji_berries_2026-0825-1311_Opus_QRS.html.
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: “Goji Berries for Health & Longevity - Quick Reference Sheet”.
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: “Goji Berries for Health & Longevity”.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 Line 421: “08/16/2026”, matching qrs_creation_date 2026-0816-1620.
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 the title and the template’s standard subline (lines 415–428); 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 lines 496–498, leading with the executable distinction “whole dried berries, not juice or an isolated extract”.
7.2 [at_a_glance] is no longer than 60 words 🟢 59 words.
7.3 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 Lipid shift, macular pigment rise and oxidative markers from ER line 496; blood sugar and vaccine response from line 496; mood/energy/sleep/waist from line 496; bleeding cases from line 498.
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 “blood fat readings”, “the yellow pigment the eye stores in its central patch”, “blood-thinning medication” — no acronyms present.
7.5 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial, author, year or sample size mentioned.
7.6 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 Only qualitative direction words (“favourably”, “substantially”, “smaller”).

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All six items trace to the ER “Populations who should avoid Goji Berries” list, ER lines 346–351.
8.2 [stop_items] represent the Contraindications from the ER 🟢 All six ER avoidance populations are present, none added.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Lines 563–571, six <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. 🟢 ER rationales stripped: “on the basis of the betaine content…”, “given the bleeding signal”, “where the antibody-shifting effect is unstudied”. No trailing dash clauses.
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). 🟢 “(regardless of INR stability)”, “within 14 days”, “with prior reaction to peach, apple or other Rosaceae fruit”, “with prior systemic reaction”, “under immunosuppression” 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 inside parentheses 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 names six such populations, and the section is correctly populated rather than empty.
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 nine items trace to ER lines 326–342.
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 Nine of the ER’s ten interaction bullets are carried; “Warfarin and coumarin anticoagulants” is correctly omitted because it appears as a contraindication.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Lines 579–593, nine <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. 🟢 Each item is the label plus its drug list; the ER’s “Caution”/”Monitor” verdicts and mechanistic sentences are stripped. No dash clauses.
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 ER example drug lists preserved verbatim; “Other interventions” gains “(time-restricted eating, very-low-fat diets)” from the ER bullet body.
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 inside parentheses 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 names ten interactions, and the section is correctly populated rather than empty.
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 trace to the ER Therapeutic Protocol bullets at lines 373, 375 and 381.
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 Standard whole-fruit dose, higher-dose macular schedule, and dosing-with-fat timing — the three the ER itself supports best; the juice and isolated-polysaccharide protocols are the two the ER explicitly discounts.
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 names more than three actionable implementation aspects.
10.4 All used [action_#label], [action#value], [action#_sub] items are filled with meaningful content derived from the ER Protocol section. 🟢 Lines 450–481: all nine action variables carry ER-derived content, none placeholder.

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 🟢 Plasma pigment (28 days), macular pigment density (90 days) and lipid changes (45 days) are exactly the three intervals given at ER line 430.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Plasma zeaxanthin (2.5-fold rise, ER line 166) precedes macular pigment density, which precedes the smaller lipid shift (0.14 mmol/L triglycerides, ER line 160).
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 provides at least three distinct time-to-effect aspects.
11.4 All used [time_#label], [time#value], [time#_sub] items are filled with meaningful content derived from the ER. 🟢 Lines 491–520: “More than double”, “Nothing here is perceptible within a week” and “Established by 16 weeks” are all drawn from ER line 430.
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 430.

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 All eleven entries map to ER subsection headings at lines 156–234.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four spans present and populated (lines 529–553), matching the ER’s four tiers.
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. 🟢 Entries are the bare ER headings joined by semicolons; no Magnitude figures, trial names or mechanisms carried through.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses appear in any benefits entry; the ER’s “⚠️ Conflicted” markers are also dropped.
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 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 nine entries map to ER subsection headings at lines 258–306.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four spans present and populated (lines 605–622), matching the ER’s four tiers.
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. 🟢 Entries are the bare ER headings; INR figures, hazard quotients and case-report detail are all omitted.
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 entry.
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 contain items in the ER.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 Table reproduces the ER Monitoring Protocol & Defining Success biomarker table, lines 458–468.
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All nine ER biomarkers present with matching targets and rationales: triglycerides, HDL cholesterol, fasting glucose, HbA1c, ALT, GGT, macular pigment optical density, INR, hs-CRP.
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. 🟢 Lines 749–754 reproduce the ER’s baseline panel and the 8-week / 16-week / 6–12-month / 6-month / annual schedule from ER line 456.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 All five items trace to the ER “Qualitative markers worth tracking” list, lines 472–476.
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All five ER qualitative markers present at lines 763–786, none omitted or added.

Issues 16/08/2026 16:31

Pass rate 100.00%. No issues found.

Issues 16/08/2026 16:26

  1. 9.4 — Trailing clause on interaction item: The Key Interactions item at line 593, “Carotenoid supplements (lutein, zeaxanthin, astaxanthin, beta-carotene): redundancy, not harm”, carries a trailing explanatory clause after the colon, which item 9.4 requires to be stripped.

Fixes 16/08/2026 16:26

  1. 9.4 — Interaction item trailing clause: Stripped the trailing explanation from the carotenoid supplements gate item, from “Carotenoid supplements (lutein, zeaxanthin, astaxanthin, beta-carotene): redundancy, not harm” to “Carotenoid supplements (lutein, zeaxanthin, astaxanthin, beta-carotene)”.