
VAPE COMPLIANCE
Triverity Laboratories supports notifications to the EU Tobacco Products Directive (TPD), the UK Tobacco and Related Products Regulations (TRPR), US Premarket Tobacco Product Applications (PMTA), and Emirates Authority for Standardization and Metrology (UAE.S 5030:2018).
Using a network of ISO/IEC 17025:2017 accredited laboratories and consultants, Triverity provides a full-service offering to help our customers achieve full compliance. Our senior analytical team conducts a comprehensive review and provides approval for Certificates of Analysis and Conformity. A project outline is designed for each product (range) to suit its specific needs and compliance with regional requirements.
We go above and beyond the industry standards to ensure you and your customer have full confidence in the quality and compliance of your products.

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Customers are set up in our online portal – all products submitted will follow a simple logging-in process
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Each product (range) goes through our initial consultation process and a project outline is subsequently designed by our expert team
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Pre-market products will be screened before commencing the required testing and compilation of regulatory documentation
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Post-market products are supported through batch testing, adverse effects, and reporting, annual sales notifications, and submission updates
ONBOARDING & PROJECT SCOPE
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2mL Fill Volume
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Nicotine Content
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Nicotine Impurities
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Nicotine Content of Vapour
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Nicotine Dose Consistency
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Puff Count
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Emissions
LABORATORY TESTS
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Density
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pH
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Viscosity
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Device Testing
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Nitrosamines
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Micro
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Particle Size
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Heavy Metals
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Extractables and Leachables
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Stability Studies
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Technical Dossier
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Gap Analysis
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SOP Generation
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GMP / ISO Accreditation
CONSULTANCY SERVICES & STUDIES
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TPD Submissions
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PCN Submissions
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Toxicological Assessment
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SDS Generation
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Packaging Review
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Label Review
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Submission Updates
INDUSTRIES SERVED
FOOD & BEVERAGE
NICOTINE
ADAPTOGENS
PHARMACEUTICAL
COSMETICS
NUTRACEUTICAL
CPG
CANNABINOIDS
VAPE
MUSHROOMS
HONEY
TOPICALS
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