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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.

Medical Device Manufacturing – Quality System Regulation (21 CFR Part 820)
FDA
Establishes quality system requirements for medical device manufacturers covering design, production, testing, and distribution processes.
December 5, 2025
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Medical Device Manufacturing – Quality System Regulation (21 CFR Part 820)
FDA
US
December 5, 2025
What it checks
•
Design Controls – Requires documented design plans, input/output specifications, design verification and validation, risk analysis, and design transfer procedures before production.
•
Records & Documentation – Requires device master records (DMR), device history records (DHR), quality system records, and complaint files maintained per specified retention periods.
•
Production & Process Controls – Mandates written procedures for device specifications, production methods, equipment maintenance, environmental controls, and process validation with statistical techniques.
Where it applies
Industries:
Pharma & Healthcare
Content types:
Packaging & Labeling, Legal & Regulatory, Product Descriptions
Channels / platforms:
Packaging, Retail
Medical Device Clinical Investigations – Investigational Device Exemptions (IDE) (21 CFR Part 812)
FDA
Regulates clinical investigations of medical devices requiring investigational device exemptions, including sponsor responsibilities, IRB oversight, and reporting requirements.
December 5, 2025
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Medical Device Clinical Investigations – Investigational Device Exemptions (IDE) (21 CFR Part 812)
FDA
US
December 5, 2025
What it checks
•
Application Requirements – Sponsors must submit IDE applications containing investigational plans, prior investigation reports, and device descriptions before beginning clinical studies of significant risk devices.
•
Records & Reporting – Mandates comprehensive record-keeping including device disposition, adverse events, subject complaints, and progress reports; requires FDA notification within 5 working days of serious unanticipated adverse device effects.
•
IRB Approval & Oversight – Requires institutional review board approval for all investigations, with continuing review at intervals appropriate to risk level but not less than annually, and immediate reporting of adverse effects.
Where it applies
Industries:
Pharma & Healthcare, Technology & Saas
Content types:
Packaging & Labeling, Legal & Regulatory, Product Descriptions
Channels / platforms:
Packaging, Retail
In Vitro Diagnostic Products – Labeling & Manufacturing Requirements
FDA
Regulates labeling, manufacturing, and distribution requirements for in vitro diagnostic products for human use, including reagents and test systems.
December 5, 2025
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In Vitro Diagnostic Products – Labeling & Manufacturing Requirements
FDA
US
December 5, 2025
What it checks
•
Labeling Requirements – Product labels must include proprietary and established names, intended use, quantity/concentration of ingredients, adequate directions for use, and applicable warnings and precautions.
•
Distribution Controls – Restricts sale and distribution of analyte specific reagents to clinical laboratories certified under CLIA and qualified entities, with specific requirements for over-the-counter drug testing collection systems.
•
Manufacturing Standards – Manufacturers must establish product specifications, conduct performance testing, maintain batch records, and implement quality control procedures to ensure product reliability and safety.
Where it applies
Industries:
Pharma & Healthcare
Content types:
Packaging & Labeling, Product Descriptions, Legal & Regulatory
Channels / platforms:
Retail, Ecommerce, Packaging
Dietary Supplements – Manufacturing & Quality Control
FDA
Establishes current good manufacturing practices for dietary supplement production, including quality control, testing, and facility requirements.
December 5, 2025
Learn more
Close
Dietary Supplements – Manufacturing & Quality Control
FDA
US
December 5, 2025
What it checks
•
Quality Control System – Requires manufacturers to establish and implement production and process control systems with written procedures, specifications for components and finished products, and reserve sample retention (typically 1 year past product expiration).
•
Testing & Documentation – Requires representative sampling, laboratory testing to verify specifications are met, material review procedures for deviations, and comprehensive recordkeeping of all manufacturing and quality control activities.
•
Personnel & Facility Standards – Mandates qualification requirements for supervisors, hygiene practices to prevent contamination, and sanitation protocols for physical plants, equipment, and utensils used in manufacturing operations.
Where it applies
Industries:
Pharma & Healthcare, Consumer Goods (CPG)
Content types:
Packaging & Labeling, Product Descriptions, Legal & Regulatory
Channels / platforms:
Retail, Ecommerce, Packaging
Dietary Supplements – New Dietary Ingredient Safety
FDA
Regulates safety requirements and pre-market notification for new dietary ingredients introduced after October 15, 1994.
December 5, 2025
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Dietary Supplements – New Dietary Ingredient Safety
FDA
US
December 5, 2025
What it checks
•
Pre-Market Notification – Requires manufacturers to submit safety information to FDA at least 75 days before introducing a new dietary ingredient into interstate commerce, including evidence that the ingredient will reasonably be expected to be safe under recommended conditions of use.
•
Anabolic Steroid Screening – FDA must notify DEA when new dietary ingredient submissions contain inadequate safety data for articles that may be or contain anabolic steroids or analogues, including product and manufacturer information.
•
Grandfather Exception – Exempts dietary ingredients marketed in the United States before October 15, 1994 from new dietary ingredient requirements, provided they are used in the same form and have not been chemically altered.
Where it applies
Industries:
Pharma & Healthcare, Food & Beverage, Consumer Goods (CPG)
Content types:
Packaging & Labeling, Product Descriptions, Legal & Regulatory
Channels / platforms:
Retail, Ecommerce, Web, Packaging
Electronic Records & Signatures – FDA Regulatory Submissions (21 CFR Part 11)
FDA
Establishes criteria for FDA acceptance of electronic records and electronic signatures in regulatory submissions and compliance documentation.
December 5, 2025
Learn more
Close
Electronic Records & Signatures – FDA Regulatory Submissions (21 CFR Part 11)
FDA
US
December 5, 2025
What it checks
•
System Validation – Requires validated systems with audit trails, operational checks, and authority checks to ensure authenticity, integrity, and confidentiality of electronic records.
•
Documentation Controls – Mandates secure, computer-generated, time-stamped audit trails for record creation, modification, and deletion that cannot be obscured or deleted.
•
Electronic Signatures – Must be unique to one individual, not reusable or reassignable, and linked to records to prevent falsification (biometric or password combinations required).
Where it applies
Industries:
Pharma & Healthcare, Food & Beverage
Content types:
Ads & Social Media, Web & SEO Content, Packaging & Labeling, Product Descriptions, PR & Press Releases, Email & CRM, Print Materials, Video & Multimedia, Retail & In-Store, Legal & Regulatory
Channels / platforms:
Web, Email

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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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