Assisting clinical researchers to achieve site study objectives is the main focus at IMARC. Expect to find the support, proof and assurance you need to overcome chaos caused by complexity while achieving compliance through consistency. Here's how:
CONTROL. Take more of it.
Leverage cost-effective monitoring, auditing and training services to stay in command from start to finish.
COMPLIANCE. Your struggle stops here.
Overcome instability created by overworked, undermanned or inexperienced staff during specific study stages.
COMPETENCE. Knowledge you can trust.
Enjoy the security of knowing that sites monitored from the start by IMARC have never received a warning letter.
CREATIVITY. Accelerate progress.
Count on our ability to critically think through issues that yield creative solutions.
COMMITMENT. Set the highest site standards.
Focus on your research while we handle logistics and logjam prevention.
This is only the beginning of how we’ll earn your approval.
For additional information on IMARC Research, please contact John E. Lehmann at 440.801.1540.