Automated Regulatory Packaging & Label Compliance AuditorNoor Siddiqui
Deterministic AI Vision & Rule Engine for FDA 21 CFR and UAE MoIAT Label Compliance.
Eliminate the multi-million dollar risk of FDA warning letters, Class I/II recalls, and UAE MoIAT customs rejections with an automated, deterministic regulatory compliance engine.
Built for wellness brands, CPG manufacturers, and regulatory consultancies requiring zero-hallucination compliance verification.
What this package includes:
Multimodal Ingestion Pipeline: Accepts vector packaging artwork (PDF, PNG, JPG) with high-accuracy layout and OCR parsing.
Deterministic FDA 21 CFR Ruleset:
§101.93 Disease Claims Prohibition (strictly flags unauthorized therapeutic claims while preserving mandatory negative disclaimers).
§101.93(c) Mandatory DSHEA Disclaimer validation.
§101.105 Net Quantity Dual-Unit verification (US Customary + Metric).
FALCPA & FASTER Act 9-Major Allergen Syntax validation.
UAE MoIAT & GSO 9:2013 Ruleset:
Clause 4.1 Mandatory Arabic Language verification.
GSO 150-1 Day/Month/Year (DD/MM/YYYY) expiry date stamping check.
Country of Origin and importer registration verification.
Tamper-Evident Cryptographic Proof: Every audit outputs a SHA-256 audit seal over detected violations and metadata.
Production Microservice: FastAPI backend with OpenAPI documentation, 100% automated test coverage, and Docker containerization.
Operating Doctrine: "No evidence, no done." Built on 16+ years of international trade, compliance, and enterprise systems engineering.
Starting at$3,500
Duration2 weeks
Tags
FastAPI
AI
Automations
Compliance
Service provided by
Noor Siddiqui Dubai - United Arab Emirates
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Automated Regulatory Packaging & Label Compliance AuditorNoor Siddiqui
Starting at$3,500
Duration2 weeks
Tags
FastAPI
AI
Automations
Compliance
Deterministic AI Vision & Rule Engine for FDA 21 CFR and UAE MoIAT Label Compliance.
Eliminate the multi-million dollar risk of FDA warning letters, Class I/II recalls, and UAE MoIAT customs rejections with an automated, deterministic regulatory compliance engine.
Built for wellness brands, CPG manufacturers, and regulatory consultancies requiring zero-hallucination compliance verification.
What this package includes:
Multimodal Ingestion Pipeline: Accepts vector packaging artwork (PDF, PNG, JPG) with high-accuracy layout and OCR parsing.
Deterministic FDA 21 CFR Ruleset:
§101.93 Disease Claims Prohibition (strictly flags unauthorized therapeutic claims while preserving mandatory negative disclaimers).
§101.93(c) Mandatory DSHEA Disclaimer validation.
§101.105 Net Quantity Dual-Unit verification (US Customary + Metric).
FALCPA & FASTER Act 9-Major Allergen Syntax validation.
UAE MoIAT & GSO 9:2013 Ruleset:
Clause 4.1 Mandatory Arabic Language verification.
GSO 150-1 Day/Month/Year (DD/MM/YYYY) expiry date stamping check.
Country of Origin and importer registration verification.
Tamper-Evident Cryptographic Proof: Every audit outputs a SHA-256 audit seal over detected violations and metadata.
Production Microservice: FastAPI backend with OpenAPI documentation, 100% automated test coverage, and Docker containerization.
Operating Doctrine: "No evidence, no done." Built on 16+ years of international trade, compliance, and enterprise systems engineering.
$3,500