The IMARC Advantage?

What makes a company unique? Why should you choose IMARC for your clinical study? These are legitimate questions that we are glad to answer. Over the past decade, IMARC has focused on meeting and exceeding our customers’ expectations. We have built our company to ensure that our team of professionals is highly competent in the area of regulatory compliance. IMARC’s strong record of compliance can be traced to our main advantage – its people.

Quality Training

A comprehensive orientation process and a high quality continuing education program equip IMARC’s staff to identify and resolve issues and remain current in the global research arena.

Meeting and Beating Deadline

Efficient and timely submission of detailed reports to sponsors over 90% ahead of deadline.

Problem-solving Abilities

Proven ability to critically think through issues during the course of the studies and formulate creative solutions.

Strong Communications

Establishing and maintaining healthy site and sponsor relationships through effective communication is an IMARC commitment.

Diversity of Staff

The IMARC staff has diverse backgrounds in a variety of areas including medicine, nursing, engineering, pharmacy, public and mental health.

Relationship Building

Excellent teamwork and synergy both internally and externally with sites, sponsors, CROs and other vendors help form important relationships helping drive productivity.

FDA Compliance Record

Over the past decade, the sites IMARC Research has monitored have not received a FDA Form 483 or warning letter.

For additional information on IMARC Research’s training and development program, please contact John E. Lehmann at 440.801.1540.