Audit: QRS - Maqui Berry for Health & Longevity

Audit conducted on 16/08/2026 00:18 using AI4L / Opus 5

Iterations

Summary

Items Count
Total 93
Passed 85
Failed 0
N/A 8
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. 🟢 Protocol doses, time-to-effect values, benefit/risk headings, contraindications, interactions, all 10 biomarker rows and the 5 qualitative markers trace to ER Therapeutic Protocol, Practical Considerations, Expected Benefits, Potential Risks & Side Effects, Key Interactions & Contraindications and Monitoring Protocol & Defining Success.
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 carries the ER’s own “no side effect has been documented” and “Trials are small and short”; no cautious ER phrasing is replaced by firmer wording.
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”). 🟢 All five avoid-populations remain in the Contraindications gate, not the Caution gate; speculative risks remain under the Speculative tier.
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. 🟢 Nothing from ER Benefit-Modifying Factors or Risk-Modifying Factors appears in the gates; gates draw solely from Key Interactions & Contraindications.
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, expert names or brand names appear anywhere in the QRS.
1.6 The QRS does not introduce new attributions. 🟢 The only attribution-like phrases (“mostly run by the sellers”, “the oxidative stress trial”, “the three-month trial”) are ER wording for the same fact.

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. 🟢 Plain, measured, evidence-first register carried over from the ER, including its explicit sponsor-bias framing.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Quantified protocol and biomarker targets alongside accessible benefit/risk phrasing.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 Content is stated as what was tested and measured, not as instruction to the reader.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 Protocol cells state doses as studied (“once daily for at least 8 weeks”), not as directives; footer disclaimer intact.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No “recommended”, “should”, or “advised” 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 file.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Technical terms are limited to established biomarker and test names (HbA1c, HOMA-IR, hs-CRP, Schirmer’s test) required by the Monitoring table.
2.8 Information is presented in a concise and very compact manner 🟢 Gate and tier items are label-level fragments; no sentence-level elaboration.
2.9 It DOES NOT address the reader directly 🟢 Confirmed by full-text check for “you”/”your”.
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. 🟢 Functional-range biomarker targets and a 10-marker panel assume a proactive, self-quantifying 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. 🟢 Meal-anchored pre-meal dosing, clinician-performed Schirmer’s testing and an 8-week course are presented without hedging on inconvenience.
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 simplified “just take a supplement” framing; standardization and monitoring requirements are foregrounded.
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 flags small, short, manufacturer-run trials; benefit tiers keep Medium as the ceiling.
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 header carries the canonical “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. 🟢 Terms such as “blood sugar” and “blood-thinning drugs” are the ER’s own headings and glossary-style wording, carried verbatim; no colloquialisms are introduced.

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 verified at lines 440, 477, 519, 539, 551, 571, 590, 594–596, 720; tier labels “Medium”/”Low”/”Speculative” unmodified at lines 525, 528, 531, 580, 583.
3.2 All “” from the [qrs_template] are present in the the QRS. 🟢 69 named spans present, covering header (4), at_a_glance, action_1–3 (9), time_1–3 (9), benefits (4), gates (2), risks (4), marker_1–10 (30), monitoring_cadence and qualitative_item_1–5.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 Every populated span maps to a checklist item; the non-variable template spans (website="evidence_review", website="audit", website="full_review") are untouched at lines 423, 426, 434.

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. 🟢 “Ocular protocol”, “Glycemic protocol”, “Whole-food approach” and all eight interaction labels match the ER bold labels verbatim (ER lines 270–284, 312–316).
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 Time-to-effect labels (“Tear production”, “Glucose effect”, “Oxidative markers”) are the ER’s own nouns from the Time to effect bullet; biomarker names copied verbatim from the ER table.
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). Color and emphasis are conveyed through CSS and bold labels. 🟢 Full-text scan returns no emoji; the ER’s “⚠️ Conflicted” marker was 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 label-level fragments; the remaining volume (10 biomarkers, 8 interactions, 5 qualitative markers) is the minimum mandated by items 9.5, 14.2 and 15.2, with no elaboration added.

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 at line 1 and before the template comment at line 16.
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 head 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: maqui_berry_2026-0825-2236_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: 2026-0816-0010.
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” is a single word with no version or qualifier.
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” is 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 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. 🟢 All eight keys are single-line, trimmed; quoting used only where YAML requires it.

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: “Maqui Berry for Health & 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: “Maqui Berry for Health & Longevity”.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 Line 421: “08/16/2026”, the correct reformatting of 2026-0816-0010.
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 subline; the ER’s “Also known as” list is 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 🟢 Line 433 condenses the ER Conclusion (ER lines 440–444): the two human-tested claims, trial quality, sponsor bias, safety silence.
7.2 [at_a_glance] is no longer than 60 words 🟢 58 words.
7.3 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 “Chilean berry … delphinidin” (ER 440), “Two claims rest on human testing” (ER 440), “small and short” (ER 440), “mostly run by the sellers” (ER 444), “no side effect has been documented” (ER 442).
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 No acronyms; “delphinidin” is introduced in place as “the deep purple pigment”, mirroring the ER’s own gloss.
7.5 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial name, year, sample size or p-value appears.
7.6 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 Effects are described directionally (“raises”, “blunts”) with no numbers.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All five items come from the “Populations who should avoid Maqui Berry” list at ER lines 288–292.
8.2 [stop_items] represent the Contraindications from the ER 🟢 All five ER avoid-populations are present; none omitted, none added.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Lines 542–546, five <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 trailing clause after the em-dash on the pregnancy bullet (“no safety or efficacy data exist…”) is stripped; no dashes remain in any item.
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 14 days” / “within 7 days”, “below 50 × 10⁹/L”, “without continuous or frequent glucose monitoring” and “Elaeocarpaceae-family” all preserved.
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 names five such populations and the section is correctly populated, not 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 eight items map one-to-one to the ER bullets at lines 270–284.
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 No overlap with the five contraindication populations; the type 1 diabetes contraindication and the insulin/sulfonylurea interaction are distinct ER entries.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Lines 554–561, eight <li> elements.
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 mitigation and consequence clause (“Caution; additive glucose lowering…”, “Mitigation is…”) is stripped; only label plus drug examples 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). 🟢 All named drug and supplement examples preserved, including “fish oil above 3 g/day”; the NSAID parenthetical is trimmed to its examples as permitted.
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 names eight 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 derive from ER Therapeutic Protocol lines 312–316.
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 The ER’s two dosing protocols (ocular, glycemic) plus the whole-food alternative are the only implementation-level bullets; the remaining bullets are background rather than actions.
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 three distinct 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. 🟢 “60 mg/day”, “180 mg/day, or 200 mg pre-meal” and “2–5 g/day berry powder” with their subs match ER lines 312, 314, 316 exactly in substance.

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 🟢 Tear production, glucose and oxidative markers are the only three time-to-effect facts in the ER (line 367).
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Tear production and post-meal glucose are the two Medium-tier benefits and lead; oxidative markers (Low tier) follow.
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 three distinct 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. 🟢 “30 days”/”larger at 60 days”, “30–60 minutes”/”Acute, following a single dose”, “4 weeks”/”daily extract” all trace to ER line 367.
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 🟢 All ten items are the ER’s benefit headings from lines 140–194.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four spans present at lines 521, 524, 527, 530.
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. 🟢 Each item is the bare ER heading; no Magnitude figures, p-values or sample sizes 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 benefit 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. 🟢 The ER has no High tier and [benefits_high] carries style="display: none" with an explanatory comment (lines 521–523).

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 All seven items are the ER’s risk headings from lines 216–252.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four spans present at lines 573, 576, 579, 582.
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. 🟢 Each item is the bare ER heading; the ER’s Magnitude paragraphs (e.g., “60–90%” iron figure) are not 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 risk 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. 🟢 The ER has neither a High nor a Medium risk tier; both spans carry style="display: none" with explanatory comments (lines 573–578).

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 The table reproduces the ER Monitoring Protocol & Defining Success table at lines 397–408.
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All ten ER biomarkers present with verbatim ranges and reasons: fasting glucose, HbA1c, fasting insulin, HOMA-IR, hs-CRP, oxidized LDL, LDL cholesterol, Schirmer’s test, tear break-up time, ferritin.
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 714 condenses ER line 395: baseline, metabolic panel at 12 weeks then every 6–12 months, tear measurements at 8 weeks, ferritin annually.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 Items come from the ER’s “Qualitative markers worth tracking” list at lines 412–416.
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All five ER qualitative markers present; only the trailing attribution on the fifth (“the outcome suggested by the heart rate variability trial”) is stripped.

Issues 16/08/2026 00:18

Pass rate 100.00%. No issues found.