Breakthroughs In Medicine And Healthcare Begin With
Research - Clinical Studies
You can become a crucial part of the future of medicine and scientific advancements
With over 15 years of delivering world-class phase II and phase III clinical research for pharmaceutical companies; AMR Conventions Research has been raising the bar on industry standards for more than a decade; all while setting its sights on the future of how we can help improve and extend patients’ lives.
Why participate?
Clinical Trials help to shape the future of medicine and health care. By taking part in a research study, you will not only be contributing to the development of investigational drug for any specific medical disorder but also help researchers in expanding the boundaries of our established knowledge.
Your decision to take part is personal and should be carefully considered. It is very important to clinical team that you understand the potential benefits and risks of participation in any research study.
Taking part in a clinical research study does not guarantee your condition will improve but potential benefits are free of cost study-related physical exams, laboratory tests, compensation for time and travel, study medications and gain a better understanding of the medical condition.
Current Clinical Studies
Major Depressive Disorder
(18-65 Years Old)
Treatment-Resistant Depression
(18-65 Years Old)
(18-65 Years Old)
Previous Clinical Trials
Treatment Resistant Depression
(18-70 Years Old)
Adult Post Traumatic Stress Disorder (Ptsd)
(18-60 Years Old)
Major Depressive Disorder Study For Adults
(18-65 Years Old)
Bipolar I Depression
(18-65 Years Old)
Adult Post Traumatic Stress Disorder (Ptsd)
(18-65 Years Old)
Pediatric And Adolescents Attention Deficit Hyperactivity Disorder (Adhd)
(6-11 & 12-17 Years Old)
Clinical Research Services
We have a diverse and experienced clinical team made up of board-certified psychiatrists, psychologist and certified physician assistants with extensive clinical research experience. Moreover, the team is complemented by the organization and efficiency of our study coordinators.
We offer the following services:
- Clinical Trial Design & Conducting Clinical Trials
- Subject Data management
- Regulatory submissions
- In-house study start up services (Regulatory submissions, contract and budget negotiations
Our site is located in a safe, professional building with plenty of parking and easy access to expressways and airports. It is also equipped with a secured medication room, fully functional lab, washroom, kitchen and a conference room for monitor visits.
Sponsor a study
Science-driven, GCP trained and transparent; our clinical team can assist you in satisfying a wide rage of regulatory and study-specific tasks. With over 15 years of experience in conducting and designing clinical trials, we have successfully conducted and completed more than 25 studies for various sponsors.
A close affiliation with community-based psychiatry practices gives us access to a database of potentially qualified study subjects to enhance study recruitment. Our medical staff; whether dealing with the sensitivity of patients in our community or the time crunched schedule of our doctors, adhere to the basic principles of data safety, confidentiality and professionalism. We are committed to providing the most up-to-date, accurate and timely medical information gathered from subject testing; all to produce potential therapeutic breakthroughs.