Preclinical Services from Feasibility to Pivotal GLP Studies
Throughout your product development process, Surpass operates in compliance with all applicable federal and state regulations. From early development to pivotal GLP compliant safety studies, we provide the preclinical research experience and scientific integrity to support your commercialization strategy.
Surgical Modeling Capabilities
| Routes of Delivery | Test Article Evaluations | Test Device Evaluations | Cardiovascular Models | Other Experimental Models |
|---|---|---|---|---|
|
Intravenous Intraarterial Intracardiac Gastrointestinal Intramuscular Transdermal Topical Oral Surgical |
Cellular Therapy Anticoagulants Antithrombotics Growth Factors Drugs Biologics Drug-Eluting Devices |
Grafts Heart Valves Tissue Sealants Stents Access Ports Ventricular Assist Tissue Stapling Vascular Closure Catheters Extracorporeal Intravascular Filters Orthopedic Prostheses Nerve Stimulators |
Acute Myocardial Ischemia Reperfusion Chronic Myocardial Ischemia Reperfusion Restenosis CABG Intracardiac Pacing Graft Failure Aneurysm Defects Septal/Ductal Defects |
Orthopedic Wound Healing Organ Transplant Urethral Bulking Toxicology Pharmacology Gastrointestinal Urologic |
To learn more about Surpass and our preclinical services, please contact us.
Call Surpass today for your preclinical research needs:
(715) 294-4371