Clinical Research Organization

“I highly recommend working with L3.  They are extremely creative and flexible in helping small companies plan, budget, and conduct internal and external performance validations on our in vitro diagnostic instruments and assays.  Additionally, they helped us recruit and schedule users for our Human Factors validation study and helped us plan and prepare for our post-market studies at various global sites.  From start to finish, the team provided invaluable guidance on regulations, Good Clinical Practices, and study protocols to help ensure compliance.  In addition, L3 was proactive, highly responsive and worked with us to accommodate product changes and site requirements while maintaining very positive relationships with our sites and investigators.  They integrated their services with our team and facilitated open communications.  Above all, they helped establish and advance our clinical trial processes and expertise to prepare us for future studies.  I truly appreciate their support, integrity, and commitment to helping their clients in any way they can.”

– Kim Walker, MS, RAC (US & EU), FRAPS, VP, Regulatory, Quality, and Clinical Affairs, Hycor Biomedical

Reach out to L3 today!