Frequently Asked Questions

Eastern Research Trials is a medical research and development company that focuses on innovative solutions to improve human health.

Eastern Research Trials offers a range of products and services including medical device development, clinical trial management, regulatory consulting, and scientific writing.

Eastern Research Trials was founded in 2005 and has been providing quality medical research and development services for over 15 years.

 Our screen failure rate is below 10%, demonstrating our commitment to accurate patient selection and high-quality data throughout the trials. 

  We have a highly trained team that follows rigorous quality protocols and oversight throughout the entire research process. We perform constant quality controls to ensure that the data collected is accurate and reliable.  

 Yes, there can be several benefits to volunteering for a clinical trial. Participants may receive access to cutting-edge treatments and medications that are not yet widely available. Clinical trial participants are also closely monitored by medical professionals, which can provide additional care and attention. Furthermore, your participation contributes to the advancement of medical research that could help others in the future. 

 In a clinical study, participants are carefully monitored by healthcare professionals throughout the trial. Depending on the study, participants may be given a new treatment or medication, or they may receive a placebo. Regular check-ups, tests, and assessments are conducted to track the participant’s health, response to the treatment, and any side effects. The data collected from these studies helps to determine the safety and effectiveness of the treatment. 

  Qualification for a clinical trial depends on specific criteria related to your age, health status, medical history, and the study's goals. Each trial has inclusion and exclusion criteria that help determine whether a person is eligible. If you are interested in participating in a clinical trial, the research team will evaluate your eligibility through an initial screening process to determine if you meet the study requirements. 

 Before participating in a clinical research study, it’s important to consider factors such as the potential risks and benefits, your personal health condition, the time commitment, and the possible side effects of the treatment being tested. It’s also important to fully understand the study's purpose, procedures, and any potential discomfort or harm. Make sure to discuss these aspects with your healthcare provider and the research team to make an informed decision.