|
 |
 |
 |
With a wealth of preclinical medical device expertise, state-of-the-art facility, and the most advanced imaging technology, APS is the Contract Research Organization of choice for in-vivo medical device testing. APS has the ability to perform GLP studies for regulatory submissions as well as feasibility research, device training, and educational programs using acute and chronic research models. |
APS affords a medical device company the ability to perform cutting-edge preclinical research without encumbrances regarding proprietary information and public disclosure. |
|
| We at APS are dedicated to: |
- Supporting medical device testing with experienced personnel and the most advanced imaging technologies.
- Accommodating a demanding schedule including fast track study initiation.
- Fostering frequent, open communication during all phases of a study.
- Managing the integrity, compliance, timeliness, format, and confidentiality of your data.
|
|
Our total commitment to these concepts will facilitate your product development and commercialization goals, ultimately advancing safe and efficacious patient healthcare. |
|
|
|
|
|
|
|
