Superior access, service, quality and deliverables in preclinical testing.

T3 Labs is a trusted, proven industry leading preclinical CRO for medical device and other medical products.  We’re an AAALAC accredited facility that conducts feasibility, proof of concept, safety, and GLP medical device testing for studies in any therapeutic area and in small and large models. Since January 2012, we have archived more than 50 GLP studies for leading medical device manufacturers of which more than 25 products have received regulatory approvals.

In Our Sponsors' Own Words

T3 Labs’ cardiology / cardiothoracic preclinical testing experience includes interventional, structural heart, electrophysiology, and renal nerve ablation technologies. Our preclinical, GLP work for leading cardiology/cardiothoracic device manufacturers employs a wide-variety of techniques such as in vivo vascular function or reactivity, and models of ischemia.

For our cardiothoracic preclinical medical device testing and training sponsors, our preclinical CRO employs the most appropriate, efficient model needed. Our GLP and AAALAC accredited facility includes a real life cath lab, high quality operating rooms and all of the equipment needed. Read more on our preclinical for cardiothoracic device page.

T3 Labs’ orthopaedic preclinical testing experience includes spine, large joints, and extremities treated with devices, biologics and cell-based products. Models include, but aren’t limited to: Spine fusion, degenerative disc disease, orthopaedic infection, tendon repair/replacement, fracture healing and critical-sized defect models.

What you need, when you need it
For our orthopaedic manufacturers / sponsors needing high quality preclinical orthopaedic device testing and training, our preclinical CRO employs the most appropriate, efficient model needed. Our GLP and AAALAC accredited facility includes high quality operating rooms and all of the equipment needed including: Digital x-ray, Micro-CT, MRI and CT, surgical instrumentation and qualified plastic histology labs. Model development is available.

Read more on our preclinical for orthopaedic device testing page.

T3 Labs’ general surgical testing experience for preclinical includes gastrointestinal, wound healing and organ transplant to name a few.

For our general surgery sponsors needing high quality preclinical device testing and training, our preclinical CRO employs the most appropriate, efficient model needed. Our GLP and AAALAC accredited facility includes high quality operating rooms and all of the equipment needed including ECHO including ICE, TTE and TEE, C-arms and MRI and CT. Model development is available.

Read more on about our preclinical testing and training programs for general surgery, urology and GI devices.

T3 Labs’ regenerative medicine testing experience includes products for wound healing, cardiovascular and orthopaedic applications.

For our sponsors needing medical device testing and training for new regenerative medicine therapies and devices, our preclinical CRO employs the most appropriate efficient model needed. Our GLP and AAALAC accredited facility includes high quality operating rooms and all of the equipment needed including cell culture and sorting, C-arms, ECHO including ICE, TTE, TEE, Doppler, IVUS, OCT, Micro-CT, MRI and CT.

Read more about our preclinical testing programs for regenerative medicine and wound healing.

T3 Labs has the surgical, veterinary and specialized experience needed to generate positive preclinical results for your drugs and biologics programs.

Delivery, dosage, biodistribution and toxicity are the top challenges for developers of new drugs and biologics. Particularly so, for those specific indications where current therapies are underwhelming. Heart attacks, critical limb ischemia, wound healing, stroke and ALS (amyotrophic lateral sclerosis) are a few of the unmet medical needs that will require new, innovative approaches for better treatments and eventual cures. T3 Labs has the unique capabilities to accelerate the development of tomorrow’s breakthrough drugs and biologics.

Read more about our Drug & Biologics programs.

T3 Labs’ preclinical testing experience in other fields includes, dermatology, neurology, and urology.

Dermatology models for preclinical include wound healing in normal or diabetic models and air pouch models.
Neurology models for preclinical include stroke and traumatic brain injury models.
Urology models include for preclinical renal calculi, street urinary incontinence, and embolic delivery models.

For medical device and pharmaceutical manufacturers of all sizes T3 Labs provides high quality, high value medical device testing, training and translational facilities. T3 Labs provides physicians, sales staff, students and allied healthcare professionals what they need, when they need it with the highest quality service designed with your training needs in mind.

Learn more about our training programs. 

Precision

T3 Labs is trusted by regulatory bodies and leading medical device product developers to deliver the highest quality preclinical GLP and non-GLP raw data and reports for medical device testing.

Quality

Our preclinical study directors/investigators are scientists with deep knowledge in their areas of expertise, pursuing their areas of greatest interest in close alignment with the needs of medical device manufacturers.

Access

We have a broad network of CRO industry leaders for medical device study design and execution including access to trusted resources via partners at Emory University and Georgia Institute of Technology.

Service

T3 Labs Program Leaders provide what you need, when you need it and ask the right questions of your medical device product developers and research engineers in advance of preclinical testing to ensure your medical device or other medical product project is approval ready.

Since January 2012, we have archived more than 50 GLP studies from which more than 25 products have received regulatory approvals. Among more than 30 studies completed, ALL returned from the FDA “ZQA,” zero questions asked.

From preclinical testing of LVADs to in-vivo micro CT and beyond, our medical device testing program leaders possess over 50 combined years of experience across 10 therapeutic specialties.

Through additional consultants/vendors including the “device design and prototyping shop” Global Center for Medical Innovation (GCMI) ac T3 creates seamless simplicity and economy via one engagement that eliminates the need for additional contracts with other physicians, CRO or labs.

Have you thought about manufacturing? What does the clinician think? Our goal is to accelerate the FDA or other regulatory approval process helping medical device manufacturers reach the next critical decision point or milestone as quickly and effectively as possible.