Surpass Ability: Knowledge and Quality Based Confidence

Our confidence is based on extensive knowledge of a wide range of targeted therapeutic areas and treatment techniques. Surpass leverages core knowledge and experience to recommend unique study methodologies. Surpass provides experience-based counsel that presents new approaches for preclinical evaluation to support your commercialization decisions.

Our comprehensive range of integrated development services are recognized to be of superior value by our sponsors in the cardiovascular, peripheral vascular, regenerative medicine, neurovascular, orthopedic, urologic, gastrointestinal, and wound healing specialties.

The keystone of our broad-based experience is our quality system which is constantly evolving to meet the ever-changing regulatory demands inherent to the industry. Surpass' quality infrastructure mitigates risk and ensures compliance with Food and Drug Administration (FDA) and United States Department of Agriculture (USDA) regulations. Surpass is a GLP compliant, AAALAC accredited, and USDA registered laboratory. Our Quality Assurance Unit (QAU) safeguards regulatory compliance by conducting critical phase audits, and routine process, facility, and vendor inspections.

Our study initiation, in-life and report process:

• Identifies your objectives and critical endpoints
• Invests planning time upfront to develop a well designed protocol that reduces unforeseen study challenges and deviations during study conduct
• Offers integrated study teams allowing for rapid decision making
• Ensures timely draft and final reports

To learn more about why the Surpass experience and process inspires confidence, please contact us.