Resources
We offer you competitive prices for simple routine testing, prompt communication regarding test status and results, and experience with regulatory and biocompatibility testing services for unique product families. Find out all our medical device testing resources.
How Comprehensive Product Testing Expertise Reduces Risk for Medtech Manufacturers
When the lifesaving and lifechanging products you make are going into patients’ bodies, there is no room for error. Every medical device manufacturer knows this…
Accelerating Time to Market By Streamlining Medical Device Testing
One of the biggest challenges in medical device manufacturing is simply getting the product to market quickly. Speed to launch isn’t just about competitive advantage;…
The Benefits of Outsourcing Medical Device Product Testing
As a medical device manufacturer, you know that every product you bring to market must meet rigorous testing standards to ensure patient safety.
How To Calculate Allowable Limits For Ethylene Oxide Sterilization
Learn what ethylene oxide residuals are and how to calculate allowable limits for EtO-sterilization of medical devices and products.
Tolerable Exposure Limits For Ethylene Oxide Sterilized Medical Devices
Learn about ethylene oxide residuals and how to calculate tolerable exposure limits for EtO-sterilized medical devices and products.
Key Differences Between USP 1115, USP 1116 and USP 1211
Learn about USP regulations regarding non-sterile and aseptic processes, and sterility assurance and how these relate to regulatory testing requirements.
How To Calculate Tolerable Contact Limits For Ethylene Oxide
Learn what ethylene oxide residuals are and how to calculate tolerable contact limits for EtO-sterilized medical devices and products.
Isolators Vs. Restricted Access Barrier Systems
Learn what isolators and RABS are, and if they can be useful in the manufacturing, filling, testing, or packaging processes for medical devices.
What Are Restricted Access Barrier Systems (RABS)?
Learn what restricted access barrier systems (RABS) are and how are they useful in manufacturing or packaging processes for medical products.
Get Your Biocompatibility, EO Residuals & Microbiology Testing Outsourced Today
Are you looking for expert guidance, better communication and faster testing turnaround times compared to your current contract testing partners? Or are you simply looking for relevant testing strategies? You have come to the right place. We offer you competitive prices for simple routine testing, prompt communication regarding test status and results, and experience with regulatory and biocompatibility testing services for unique product families.
Testimonials
Christopher Lavallee
Clean Room Certs, Inc.
“Ethide personnel have been instrumental in using their direct knowledge of USP-797 to help educate our customers and ensure they receive the latest guidance and inputs that could affect their businesses. Ethide has helped our customers best determine the types of testing that would most suite them based on the direct nature of those customers work related functions. CCS would highly recommend Ethide Laboratories to other medical device manufacturing companies for their continued ability to quickly fill our sometimes-short notices requests for sampling supplies.”