+1(786)493-4013

Making the difference by high quality evidence based clinical trials

About us

Legacy MD research institute is a multi-specialty medical research site in South Miami, Florida. We work with some the world’s most prestigious pharmaceutical companies in the development of new treatments that will potentially help patients improve their conditions and quality of life. We have strong patient recruitment sources and clinical and data quality assurance process to ensure our work is accurate and complete. Our trained and dedicated staff conducts research studies for a large variety of medical specialties including internal medicine, neurology, pulmonology, colorectal surgery and psychiatry among others. Whether you are a sponsor of a clinical trial, a prospective participant, or an industry professional, we invite you to learn more about us. We look forward to hearing from you.

 We at Legacy MD Research Institute are highly dedicated to conduct clinical trials, which are essential to the development of the future, more innovative therapies. Legacy MD is proud to contribute and serve the medical community in helping to understand the diseases that affect our daily lives. Our broad range of medical specialties is committed to improve quality of life by being a trusted source for the highest degree of excellence in clinical research.

OUR TEAM

Our awesome staff are all CPR Certified.
Trained and experienced clinical research team.
24-Hour Physician On-call for Emergencies? 

Erick Juarez MD ABFM PI

Medical doctor Principal investigator 

ANA B. Rotella 

study coordinator director 

Marisely Avila 

Chief Aesthetician

what are clinical trials 

 A clinical trial is a research study in human volunteers to answer specific health questions. Carefully conducted clinical trials are the safest and fastest way to find treatments that work in people, and new ways to improve health. There are different kinds of clinical trials, including prevention options, new treatments or new ways to use existing treatments, new screening and diagnostic techniques and options for improving the quality of life for people who have serious medical conditions. Clinical trials are conducted according to a plan called a protocol. The protocol describes what types of patients may enter the study, schedules of tests and procedures, drugs, dosages, and length of study, as well as the outcomes that will be measured. Each person participating in the study must agree to the rules set out by the protocol.
2.- What are the Phases of clinical trials?
3.- Who can participate in a clinical trial?
4.- What should I think about before joining a clinical trial?
5.- As a participant, what should I expect?
6.- What are the benefits and risks of participating in a clinical trial? 7.- Does it cost money to participate in a clinical trial?
8.- Are clinical trials safe?
9.- What is informed consent?
10.- Is my health information protected in a clinical study?
11.- Who should consider clinical trials and why?
12.- What's the role of the FDA in approving new drugs & medical treatments? your description

Address

  • 4960 sw 72 ave suite 203
    miami, FL 33155

Phone

1 786-493-4013

Business Hours

  • Monday - Friday
    07:00am – 06:00pm
  • Saturday - Sunday
    Closed

Address

4960 sw 72 ave suite 203
miami, FL
US

Phone

1 786-493-4013

Email

infodesk@legacymd.org

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Legacy MD Research Institute

Address

4960 sw 72 ave suite 203
miami, FL, 33155, US

1 786-493-4013 infodesk@legacymd.org

About us

We are a dedicated research site proficient in Phase II-III-IV clinical trials in South Miami, Florida. Our diversified and extensive industry experience enables us to offer our sponsors a quality research site with a trained and experienced clinical research team. We are committed to meeting the needs of trial sponsors. From initial submission of regulatory documentation and budget development, through enrollment, data clarification and study closure, our ideal combination of experienced, highly qualified research staff and business organization allows us to respond rapidly and knowledgeably to sponsor requests. Sponsors expect sites to efficiently recruit study participants. We are allied to several physicians who offer services to the Baptist Health System of South Florida, Stuart health, Keralty hospital. our physician have hopsital privileges at the area hospital. We also have an extensive   database of over 10000 potential subjects. We promise a one-to- two week turnaround on regulatory and contract start-up. The independent status of our center allows the use of a central IRB, thus shortening the regulatory approval process and expediting many aspects of administrative studies start up and budget approval. Being a dedicated research facility eliminates the potential for scheduling conflicts with non-research patients. Our experienced full time research staff allows full concentration on the demands of the studies. Subject visit requirements are projected to determine the optimum rate at which subjects may be enrolled, to avoid a conflict with staff or facility capabilities. Whenever possible, study specific source documents which integrate Case Report Form data points are used. If required, source documents, study-tracking spreadsheets, enrollment logs, drug accountability forms and subject compliance evaluations, electronic data entry are also developed and utilized. Quality is our highest priority at Legacy MD Research Institute. Our experienced research professionals adhere to the highest ethical, regulatory and industry standards. Our informed, result-driven, and interactive approach assures sponsors that their protocols are well- managed and successful when placed at our facility.

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