Columbus Clinical Services offers clinical site solutions to pharmaceutical and biotech companies, medical device companies, and contract research organizations (CROs) looking to find research sites that will provide patients for their studies. Columbus Clinical Services is a dedicated Phase I-IV clinical research facility which can help these businesses accrue more patient samples in a shorter amount of time.
Our team of bilingual experts have years of experience conducting clinical research. Our network of qualified medical professionals and the drive of our study coordinators ensures that our studies are carried out accurately and efficiently. We take pride in upholding ethical standards, striving to complete our studies as quickly and productively as possible.
Since 2005, we have been a respected clinical study site that continues to provide top-quality service. Our patient database is unique and meets the needs of various studies. It has grown primarily through private investigator referrals, word of mouth marketing strategies, and recruitment from different ethnicities.
We strive to provide the best medical care possible for all participants, and to conduct clinical research safely, correctly, and accurately in order to build credible information for our sponsors / CROs.
Clinical trials are led by physicians, who also rely on a team of specialized professionals to help carry out the research. The goal is to find new and more effective ways of treating patients.
When you choose to take part in a clinical trial, you are helping to advance research and bring new treatments closer to patients. Your participation can lead to more comfortable treatment options as well as better understanding of the disease or illness. You will also be compensated for your time and participation.
You are an essential part of clinical trials! All types of participants are needed because some conditions can be more common in certain groups. Whether you’re young, old, white, black or have any other characteristic – clinical trials need you to participate!
The selection of study participants involves determining who may be eligible to participate in the study. Site reviews the inclusion and exclusion criteria for potential patients in order to determine a patient pool for the study.
You will be asked to sign a study consent form and receive medical information about the study. You may also need to have a physical assessment and review of your medical history. A waiting period phase may be required before you can begin the study.
A process by which the eligibility of study participants is evaluated, using criteria such as whether they meet inclusion and exclusion requirements. If a participant meets these qualifications, they may be enrolled in the trial; if not, they are excluded from participation.
During the treatment period, we will be keeping an eye on your progress and any potential side effects from the medication. Regular follow up visits to and/or labs may be necessary in order to monitor your health.
After your trial is complete, you will have one final safety check and also a slew of other tests.
Columbus Clinical Services is the perfect research facility for CROs and sponsors looking for a reliable, flexible solution. Our facility is designed to meet the needs of both small and large studies, making us an ideal choice for any clinical trial. At Columbus Clinical Services, we have a long history of providing excellent service to our clients.
We make use of the latest technologies in our studies to ensure that our research is conducted according to protocol, with reliable equipment, and under safe guidelines for all involved.
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