Register Your Toxicology Device in Brazil
Drug testing, therapeutic monitoring, toxicology analyzersโfast-track your toxicology products through ANVISA.
Free consultation โข No commitment required
30-365
Days to Market
500+
Devices Registered
60-80%
Cost Savings
10yr
Registration Validity
Toxicology IVDs Need Specialized Documentation
Specialized devices need specialized expertise
High-Stakes Results
Drug testing devices influence critical decisions. ANVISA requires rigorous accuracy and specificity data.
Method Validation Depth
Cross-reactivity, detection limits, and interference studies must be comprehensive and well-documented.
Regulatory Sensitivity
Devices used for forensic or workplace testing face additional scrutiny from ANVISA reviewers.
We Specialize in Toxicology Devices
Pure Global experts know your device category inside out
Deep Category Expertise
Comprehensive method validation documentation
Technical Documentation Excellence
Cross-reactivity and interference study presentation
Proven Registration Track Record
Therapeutic drug monitoring device expertise
Ongoing Compliance Support
Point-of-care toxicology device registration
How It Works
Free Consultation
Share your device details. We'll confirm classification, assess your documentation, and provide an exact quote.
Expert Dossier Preparation
Our regulatory specialists prepare your complete submission with deep specialty knowledge.
Submission & Management
We submit on your behalf and manage the entire review process, including deficiency responses.
Market Your Device
Receive your registration. Your device is legally marketable for 10 years.
Trusted by Leading Toxicology Device Companies
โOur workplace drug testing device is now registered in Brazil thanks to Pure Global's toxicology IVD expertise.โ
Dr. Mark Stevens
VP Product Development, ToxScreen Diagnostics
Transparent Pricing
Complete service, no hidden fees
Starting from
Starting from $2,000/year
Based on device class and complexitySave 60-80%
Ready to Register Your Toxicology Device?
Get a free consultation with our regulatory experts. We'll assess your device and provide an honest timeline and quote.