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    TVT Platform
    TVT

    Automate text and image reviews in one place. Compare any format or layout.

    TVT Artwork

    Review complex printer’s proofs and find image discrepancies that are invisible during a visual check.

    TVT Spelling

    Find all spelling errors in multilingual projects and documents with specialized terms.

    TVT Barcode

    Make sure your barcodes are readable before you go to print.

    ROI Calculator

    Estimate time and cost savings with TVT

    Try the Calculator
    Implementation & Support
    Customer Success and Training

    Guided onboarding, highly-rated support and on-demand training – all included.

    Integration

    Seamless integration across your tech stack.

  • Industries
    Core Regulated Industries
    Pharmaceutical

    Stay on top of regulatory requirements and make sure no error slips through.

    FMCG & CPG

    Speed up reviews and easily keep track of document versions.

    Medical Device

    Easily handle content comparison for IFUs, DFUs, manuals and packaging.

    Crop Science

    Simplify your workflows for high-volume text verification.

    See how TVT works for your industry

    Explore how TVT supports industry-specific content verification.

    Customer since 2025

    Faster, more accurate ISI reviews

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    The hidden complexity of global labeling: what medical device and IVD teams need to know

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Webinars

Common pitfalls of artwork creation process and how regulatory affairs teams can prevent them
Webinars
Artwork
<1 min read
by Schlafender Hase
Common pitfalls of artwork creation process and how regulatory affairs teams can prevent them
RAPS webinar: e-Labeling and what it means for regulatory teams
Webinars
RAPS Webinar
2 min read
by Schlafender Hase
RAPS webinar: e-Labeling and what it means for regulatory teams
  • View all
  • Pharma and Med Device Regulations
  • RAPS Webinar
  • TVT Highlights
  • TOPRA Webinar
  • FMCG
  • Artwork
Common pitfalls of artwork creation process and how regulatory affairs teams can prevent them
Webinars
Artwork
<1 min read
by Schlafender Hase
Common pitfalls of artwork creation process and how regulatory affairs teams can prevent them
RAPS webinar: e-Labeling and what it means for regulatory teams
Webinars
RAPS Webinar
2 min read
by Schlafender Hase
RAPS webinar: e-Labeling and what it means for regulatory teams
TVT Integration: connect, automate, accelerate
Webinars
TVT Highlights
<1 min read
by Mike Baird
TVT Integration: connect, automate, accelerate
Precision Talks: optimizing packaging workflows with compliance and innovation with Esko
Webinars
FMCG, Artwork
<1 min read
by Marc Chaillou
Precision Talks: optimizing packaging workflows with compliance and innovation with Esko
How are increased compliance requirements impacting medical devices?
Webinars
Pharma and Med Device Regulations
2 min read
by Peter Muller
How are increased compliance requirements impacting medical devices?
Learning the new language of the EMA & the FDA: FHIR
Webinars
Pharma and Med Device Regulations
2 min read
by Mike Baird
Learning the new language of the EMA & the FDA: FHIR
The role of barcodes in life sciences, and the key to ensuring barcode accuracy
Webinars
Pharma and Med Device Regulations
<1 min read
by Mike Baird
The role of barcodes in life sciences, and the key to ensuring barcode accuracy
Embracing e-Labeling in a global context
Webinars
Pharma and Med Device Regulations
2 min read
by Dr. Jutta Hohenhoerst
Embracing e-Labeling in a global context
TOPRA sponsored webcast: a non-technical AI introduction for regulatory affairs professionals
Webinars
TOPRA Webinar
2 min read
by Dean Halliday
TOPRA sponsored webcast: a non-technical AI introduction for regulatory affairs professionals
1 of 2

Helpful resources

Everything you need to stay accurate, audit-ready, and ahead of what’s changing.

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Educational docs

Downloadable glossaries, compliance checklists, infographics, and process guides designed to help teams align quickly on complex regulatory topics.

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eBooks

Step-by-step guides to improving artwork approvals, regulatory submissions, and content verification workflows across complex teams.

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