Canyon Labs is a one-stop shop for the pharmaceutical and medical device industries. As an ISO 17025-accredited laboratory, we provide turnkey services covering sterilization, analytical testing, packaging consulting & testing, and quality & regulatory assurance consulting.  

Some of our services include: 
- 510K Consulting
- EU MDR Consulting
- Packaging Design 
- Sample Size Justifications 
- Documentation Authorship for QA/RA, Packaging and more
- Extractables & Leachable
- ISO 10993 Testing
- EO Residuals
- Bioburden
- Biocompatibility / Cytotoxicity Testing 
- Routine Sterility Testing 
- E-Beam Sterilization
- ETO Sterilization
- BI Sterility
- Product Sterility 
- LAL Endotoxin
- Bacteriostasis & Fungistasis (B&F) Testing
- ISO 11607 Testing including transit, accelerated & real time aging and integrity testing

We pride ourselves in setting a new standard for service in the industry by excelling in timely turnarounds, accessible expert support, and customizable solutions for each stage of your project. Let us show you what working with trustworthy experts is like!

Contact us at info@canyonlabs.com or call 801.406.6700

Packaging Services

Pharmaceutical

Medical Devices

Canyon Labs

Sarah Rosenblum Ptach

Kyle Kempf

Clint Christensen

The Quality Assurance and Compliance team at Canyon Labs ensures that all processes and products meet rigorous industry standards and regulatory requirements. This team is responsible for overseeing quality control measures, performing equipment calibration and maintenance, coordinating compliance initiatives, and ensuring thorough documentation and adherence to ISO 17025 standards across all services. Their expertise guarantees that all deliverables are reliable, safe, and effective for pharmaceutical and medical device applications.

Quality Assurance and Compliance

About

Team members

Other teams at Canyon Labs

Leadership Team