Medical Device Testing and Validation
We’re your one-stop source for medical device testing and validation — for products, materials and packaging.
Our professional engineers and technicians provide reliable, quality-assured testing services and documentation throughout every step of the critically important testing and validation process.
A leader and innovator in the medical device testing industry, we offer single-source solutions to medical device development engineers, Quality Assurance, and regulatory affairs professionals who want to confirm that their devices meet all regulatory agency requirements and the highest industry standards.
Medical device manufacturers are required to obtain 510(K) approval on each medical device package. We perform a variety of testing services to ensure that the integrity of the medical device is compliant.
Whitehouse Laboratories has the capability to perform standardized and customized functional, mechanical, force, dimensional /metrology, and dose delivery/accuracy testing for drug delivery and medical devices. Testing can be designed to support all lifecycle phases of your combination products and packaging, from early concept and preclinical testing, to final product qualification, as well as through management of ongoing commercial program support. Whitehouse Laboratories also has the capabilities to assist with your regulatory compliance submissions with supplemental drug delivery and medical device testing, such as long-term real time and accelerated stability and container closure integrity testing.