MLRagent

Rules

24 of 251 rules

US-MIS-001·21 CFR 202.1(e)(3)(i)AI-verified
Untrue information in one part of an ad cannot be cured by truth elsewhere
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US-MIS-002·21 CFR 202.1(e)(3)(i)Disputed
Misleading omissions in prescription drug ads require added qualification within that part/theme
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US-MIS-003·21 CFR 202.1(e)(5)(iii)AI-verified
Ad must not omit facts material to its representations or to use consequences
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US-MIS-004·21 CFR 202.1(e)(6)(iii)AI-verified
No presenting since-invalidated favorable information as current
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US-MIS-005·21 CFR 202.1(e)(6)(iii)AI-verified
No literature/quotations more favorable than the evidence supports
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US-MIS-006·21 CFR 202.1(e)(6)(iv)AI-verified
No selective presentation of information to suggest greater safety than demonstrated
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US-MIS-007·21 CFR 202.1(e)(6)(v)AI-verified
No overstating the generalizability of a single study's experience
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US-MIS-008·21 CFR 202.1(e)(6)(vi)AI-verified
Disclose when effectiveness claims may reflect concomitant therapy
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US-MIS-009·21 CFR 202.1(e)(6)(vi)AI-verified
Disclose placebo-effect info when citing studies for human drug effectiveness
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US-MIS-010·21 CFR 202.1(e)(6)(viii)AI-verified
No favorable authority quote without disclosing later or concurrent unfavorable data
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US-MIS-011·21 CFR 202.1(e)(6)(ix)AI-verified
No quoting or paraphrasing out of context to mislead
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US-MIS-012·21 CFR 202.1(e)(6)(xiii)AI-verified
Studies on normal subjects must disclose that fact unless drug is for normal individuals
blockercheckable
US-MIS-013·21 CFR 202.1(e)(6)(xiv)Disputed
No misleading pooled statistics in prescription drug advertising
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US-MIS-014·21 CFR 202.1(e)(6)(xv)AI-verified
No Erroneous Use of "No Significant Difference" to Claim Equivalence
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US-MIS-015·21 CFR 202.1(e)(6)(xviii)AI-verified
No misleading headlines, subheadlines, or graphics in prescription drug ads
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US-MIS-025·Q.6/A.6AI-verified
Claims should not rest on speculation, belief, or a poorly designed or conducted study
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US-MIS-031·Section V, Q1, item 1AI-verified
Source publications that distort studies or include fraudulent data should not be disseminated
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US-MIS-032·Section V, Q4, item 1 (Reprints)AI-verified
Do not share reprints that misrepresent or overstate their findings
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US-MIS-033·Section V, Q4, item 2.a (CPGs)AI-verified
Do not share CPGs that misrepresent or overstate their underlying findings
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US-MIS-034·Section V, Q4, item 2.b (Reference Texts / Digital Clinical Practice Resources)AI-verified
Do not share reference texts or digital resource content that misrepresents or overstates findings
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US-MIS-037·Section V, Q5 (prohibited practices)AI-verified
Do not include safety/effectiveness representations inconsistent with the source publication
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US-MIS-038·Section V, Q5 (prohibited practices)AI-verified
Do not present source publication information out of context
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US-MIS-039·Section V, Q5 (prohibited practices)AI-verified
Do not use statistics/techniques to suggest significance beyond what the data supports
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US-MIS-040·Section V, Q5 (prohibited practices)AI-verified
Do not use presentational elements to obscure or distort scientific content
blockerneeds human judgment