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L3 Services

L3 supports IVD and medical device organizations from concept to beyond clearance with an experienced and highly specialized team to guide and execute your strategies.

  • Clinical trials
  • Investigator initiated studies
  • Post-market studies
  • Health economic modeling
  • Market development
  • Advisories
  • Evidence planning
  • Medical education
  • Labeling
  • Site Materials/Training Tools

Your Team

Lauren Lee (Geisbert) Lehman

Partner

Kirsten Dorsey

Partner, Director of Operations

Jane Edwards, CCRA, RAC

Director, Clinical Projects

Lara Brandon Poznak, CCRA

Clinical Trial Manager

Cheryl Kierce

Administrative Coordinator

Why Companies Love Working with L3

Clinical Research Organization

L3 is 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. Read More>>

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

EDC Design & Configuration

I would highly recommend evaluating iMedNet and allowing L3 to design and configure the system. Read More>>

Christopher L. Emery, M.D., D. (ABMM) Director, In Vitro Diagnostics Development and Clinical Trials Group, Indiana University Department of Pathology and Laboratory Medicine

Innovative Design

L3 was able to take a startup budget and deliver a design aesthetic of a Fortune 500. Read More>>

Han Chen CEO, ZeaKal, Inc.

High Quality Clinical Tools

L3 provided high quality educational and promotional tools for our target clinical audience. Read More>>

Scott Mader President & CEO, Clindevor 360

Rapid Integration

I instantly had a fully capable marketing department, for a fraction of the cost of hiring a new team from scratch. Read More>>

Jonathan Ruais Vice President, Global Marketing, Opsens
WHEN OUTSOURCING YOUR NEXT CLINICAL TRIAL…