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Regulatory compliance

Checks against industry and government rules to flag violations before anything goes live

‍

Best practices

Channel-specific guidance to reduce rejections and lift engagement

Creative compliance

Claim wording, imagery, targeting and audience suitability

Platform & channel policies

Stay aligned with evolving ad and content policies

Accessibility 
& transparency

Plain language, inclusivity, and readability checks so content is clear, accessible, and trustworthy

Brand consistency

Upload your internal rules and style guides to enforce voice, terminology, and visual identity across every asset

Regulatory compliance

Checks against industry and government rules to flag violations before anything goes live

Best practices

Channel-specific guidance to reduce rejections and lift engagement

Creative compliance

Claim wording, imagery, targeting and audience suitability

Platforma and channel policies

Stay aligned with evolving ad and content policies

Accessibility & transparency

Plain language, inclusivity, and readability checks so content is clear, accessible, and trustworthy

Brand consistency

Upload your internal rules and style guides to enforce voice, terminology, and visual identity across every asset

Find checks* that fit your needs

*Check is a set of rules grouped under one topic that checks whether content follows the requirements,
guidelines, or best practices related to that topic.

Clinical Research & Human Subjects – IRB Standards & Procedures
FDA
Establishes standards for Institutional Review Boards (IRBs) reviewing FDA-regulated clinical investigations to protect human subjects' rights.
December 5, 2025
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Clinical Research & Human Subjects – IRB Standards & Procedures
FDA
US
December 5, 2025
What it checks
•
IRB Composition – Requires at least five members with diverse expertise, including one nonscientist and one member not affiliated with the institution, to review clinical investigations.
•
Documentation & Records – Mandates retention of IRB records including protocols, meeting minutes, continuing review documentation, and correspondence for at least three years after research completion.
•
Review Criteria – IRBs must ensure risks are minimized, are reasonable relative to benefits, informed consent is obtained, and vulnerable populations receive additional safeguards.
Where it applies
Industries:
Pharma & Healthcare, Food & Beverage, Consumer Goods (CPG), Technology & Saas
Content types:
Legal & Regulatory, PR & Press Releases, Web & SEO Content
Channels / platforms:
Web, Print, Email
Plant Sterol/Stanol Ester Products – Health Claims & Heart Disease Risk
FDA
Regulates health claims linking plant sterol/stanol esters to reduced coronary heart disease risk, including daily intake requirements and labeling standards.
December 5, 2025
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Plant Sterol/Stanol Ester Products – Health Claims & Heart Disease Risk
FDA
US
December 5, 2025
What it checks
•
Daily Intake Requirements – Products must contain minimum 0.65g plant sterol esters or 1.7g plant stanol esters per serving, consumed twice daily at different times to achieve 1.3g or 3.4g daily intake respectively for CHD risk reduction.
•
Labeling & Disqualification – Products must meet nutrient thresholds (low saturated fat, cholesterol, sodium) and carry mandatory label statements about daily intake timing, qualifying populations, and physician consultation for cholesterol-lowering medication users.
•
Claim Language Standards – Health claims must state plant sterol/stanol esters "may" or "might" reduce heart disease risk as part of a low saturated fat and cholesterol diet, without attributing specific degrees of risk reduction or implying exclusivity.
Where it applies
Industries:
Food & Beverage, Pharma & Healthcare
Content types:
Packaging & Labeling, Product Descriptions, Legal & Regulatory
Channels / platforms:
Packaging, Retail, Ecommerce
Clinical Research & Human Subjects – Informed Consent & Protection Standards
FDA
Establishes requirements for informed consent, IRB oversight, and additional safeguards for children participating in FDA-regulated clinical investigations.
December 5, 2025
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Clinical Research & Human Subjects – Informed Consent & Protection Standards
FDA
US
December 5, 2025
What it checks
•
Informed Consent Requirements – Mandates disclosure of risks, benefits, alternatives, and voluntary participation rights; requires documentation except in minimal risk scenarios (waiver conditions specified in §50.23).
•
Children Protection Standards – Requires additional IRB review categorizing pediatric research by risk level; mandates parental permission and child assent; prohibits wards from participating in non-beneficial research (§50.50-50.56).
•
Emergency Research Exception – Permits waiver of informed consent when subjects face life-threatening conditions, available treatments are unproven/unsatisfactory, and obtaining consent is not feasible (requires IRB approval and community consultation per §50.24).
Where it applies
Industries:
Pharma & Healthcare
Content types:
Advertising, Marketing, E-commerce, Retail, Media, Publishing, Legal, Regulatory
Channels / platforms:
Web
Soy Protein Products – Heart Disease Health Claims
FDA
Regulates health claims about soy protein's role in reducing coronary heart disease risk when part of a low saturated fat and cholesterol diet.
December 5, 2025
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Soy Protein Products – Heart Disease Health Claims
FDA
US
December 5, 2025
What it checks
•
Minimum Soy Content – Products must contain at least 6.25 grams of soy protein per serving to qualify for the heart health claim (half the daily 25-gram recommendation).
•
Label Specifications – Claims must use specific model language formats, include serving size information, and state the amount of soy protein provided per serving toward daily needs.
•
Dietary Context Requirements – Claims must specify the product is part of a diet low in saturated fat and cholesterol, and may reference blood cholesterol as the intermediate health link.
Where it applies
Industries:
Food & Beverage, Pharma & Healthcare
Content types:
Packaging & Labeling, Product Descriptions, Web & SEO Content
Channels / platforms:
Packaging, Retail, Web, Ecommerce
Infant Formula – Nutrient Requirements & Labeling Standards
FDA
Regulates infant formula nutrient specifications, labeling requirements, quality control, and mandatory recall procedures under FDA oversight.
December 5, 2025
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Infant Formula – Nutrient Requirements & Labeling Standards
FDA
US
December 5, 2025
What it checks
•
Nutrient Specifications – Requires minimum and maximum levels for 29 nutrients including protein, fat, vitamins, and minerals (e.g., vitamin A 250-750 IU/100 kcal, iron 0.15 mg minimum).
•
Recall Procedures – Establishes FDA-required and firm-initiated recall protocols with specific notification requirements, public warnings, and effectiveness checks for contaminated or deficient products.
•
Labeling Requirements – Mandates nutrient information per 100 kilocalories, use-by date, preparation/storage directions, and warnings about improper dilution or unboiled water use.
Where it applies
Industries:
Pharma & Healthcare, Food & Beverage
Content types:
Packaging & Labeling, Product Descriptions, Legal & Regulatory
Channels / platforms:
Packaging, Retail, Ecommerce, Web
Food & Dietary Supplement Labeling – Health Claims & Cardiovascular Disease
FDA
Regulates health claims on food labels about soluble fiber reducing coronary heart disease risk and noncariogenic sweeteners preventing tooth decay.
December 5, 2025
Learn more
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Food & Dietary Supplement Labeling – Health Claims & Cardiovascular Disease
FDA
US
December 5, 2025
What it checks
•
Coronary Heart Disease Claims – Foods containing soluble fiber (from whole oats, psyllium husk, barley) may make claims about reducing CHD risk when part of a diet low in saturated fat and cholesterol, with specific serving size requirements (e.g., 0.75g soluble fiber from whole oats per serving).
•
Claim Format Requirements – Specifies mandatory language for health claims including relationship statements between diet and disease, requires disclosure of saturated fat/cholesterol content, and provides approved shortened claim versions for small packages.
•
Dental Caries Claims – Foods sweetened with sugar alcohols or specific non-cariogenic sugars may claim they do not promote tooth decay, requiring the food to be sugar-free and meet fermentability testing standards to qualify for the claim.
Where it applies
Industries:
Food & Beverage, Pharma & Healthcare
Content types:
Packaging & Labeling, Product Descriptions, Legal & Regulatory
Channels / platforms:
Packaging, Retail, Ecommerce, Web

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Explore our detailed FAQ section
for in-depth answers and insights
How does GetGenAI stay up to date with regulations?
GetGenAI connects directly to regulatory databases and trusted sources through APIs, so our Inspectors update in real time as laws, advertising codes, or platform policies change — no manual tracking or revalidation needed.
Can I add my own rules or brand guidelines?
Yes. You can upload internal rules — like brand tone, claim wording, or style guides — and GetGenAI will turn them into private Checks for your team.
What do Check results look like?
You’ll see what’s wrong or risky, why it matters, and how to fix it — often with a one-click option to apply the change automatically.
What are GetGenAI Checks?
Checks are smart rule sets built for specific needs — from industry regulations to creative best practices and brand voice. Each one reviews your content through a focused lens, like “FDA rules for health ads” or “tone and readability for SEO.”
Can I run multiple Checks at once?
Yes. Most teams combine several — for example, Regulatory + Creative + Brand Consistency — to cover all angles in one quick review.
How do I choose which Checks to use?
You can select Checks based on your industry, content type, and region, but we’ll also help you choose the right mix during your demo — tailoring them to your brand, workflows, and compliance needs.
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