Streamline your clinical trials with the help of our expert team. Partner with us!
Quality You Trust, Results You Need
KOCH Research is your trusted partner in accelerating medical advancements. We offer clinical trial services designed to streamline the process and maximize success for our sponsors and Contract Research Organization.
Mission
Our mission revolves around providing transparent, accessible and innovative clinical trial solutions to advance treatment and therapies.
Why Choose Us
Koch research prioritizes excellent compliance in clinical research, quality, and comfort of contract research organization in Morton.
Key Points:
- Dr Koch has 31 years’ experience in clinical research in a wide range of therapeutic areas related to clinical research.
- We are part of a primary care office and have great relationships with our patients that has created a proven record of excellent compliance and retention with research subjects
- We are very responsive and can expedite study startup by responding to budgets/contracts within 1 business day and submitting to the IRB within 1 week of study award
- We have a proven track record of high enrollment in In-Vitro Diagnostic (IVD) device studies and in healthy person vaccine studies
- We have the benefit of being connected to our primary care office to give us access to patients, but we also have the benefit of having a wing of our building dedicated to our research team.
- Our refrigerators, freezers (including 2 ultra-low temperature freezers), and drug storage cabinet are all connected to continuous temperature monitoring with mobile alerts.
- All study documentation and supplies are kept in a locked storage room, only accessible to the research staff.
- For high enrolling studies, we have the ability to borrow staff from our primary care office to bring in more patients. Our clinical staff are all trained on GCP for research studies.
Research Partnerships
Frequently Asked Questions
How can KOCH Research help you find qualified patients for your trial?
We leverage our extensive network of experienced clinical research sites in Illinois and diverse patient populations to identify ideal participants efficiently.
What steps do you take to ensure regulatory compliance throughout the trial?
Our experienced team stays up-to-date on regulations and meticulously manages all aspects to ensure your trial performs smoothly.
How do you handle data collection and management during the trial of CROs?
We utilize secure, state-of-the-art technology and rigorous protocols to ensure data integrity and quality throughout the entire study.
What communication channels do you use to keep us informed about the trial's progress?
We maintain open communication through regular reports, meetings, and a dedicated online portal, ensuring you have real-time access to key data and updates.
