Keeping the tip of the GLP spear sharp: SQA 2016
Remaining on the forefront of FDA requirements and learning from our peers’ experience is why we invest in the SQA Conference every year including SQA 2016.
Preclinical Case Study: St. Jude Medical & T3 Labs for CardioMEMS HF System
“At the preclinical stage of medical device product development, there is an important opportunity to identify and implement significant improvements before first clinical use. T3 Labs provides extensive expertise and capabilities in the critical preclinical stage of medical device product development.” – Jason White, Senior Director of Product Development, St. Jude Medical The challenge:…
Case Study: Selecting a New Preclinical Trials Partner – T3 Labs & ALung’s Hemolung RAS in a Calf Model
ALung Technologies needed a CRO with great flexibility and responsiveness in order to maximize limited resources and accelerate the timeline associated with preclinical trials. “T3’s recommendation has accelerated our product refinement testing and preclinical trials saving ALung time and money at every step along the way.” – Jeremy Kimmel, PhD Director of New Technology for ALung Technologies…
Top Factors Enabling Swift GLP Turnaround Under Tight Preclinical Timelines
Preclinical medical device testing: how do you know you are ready and how do you make the most efficient investment in preclinical?
Surefire Precision gains FDA 510(k) clearance twice as fast as the industry average with T3 Labs
Surefire Medical achieves FDA 510(k) clearance for direct-to-tumor embolization device Surefire Precision in just 76 days with the help of T3 Labs.