Welcome to EMPIRE-MED Clinical Trials
Advancing Medicine For Current and Future Generations.
OUR VISION
It strives to be a leading contributor to developing medicines and treatments for current and future generations while providing excellent medical services to patients.
17+
Professional Team
300+
Active Patients
5+
Enrolling Studies
WHAT IS CLINICAL RESEARCH?
The evolution of clinical research traverses a log and fascinating journey. From the first recorded trial legumes in biblical times to the first randomized controlled trial Streptomycin in 1946, the history of clinical trials covers a wide variety of challenges- scientific, ethical, and regulatory.
What are the Phases of Clinical Research?
- Pre-Clinical
- Phase I
- Phase II
- Phase III
- Phase IV
¿WHO CAN PARTICIPATE IN A CLINCIAL TRIAL?
All clinical trials have criteria that determine who is allowed to participate.
You cannot participate in a study if you don’t meet all of the study criteria. T
WHAT HAPPENS DURING A STUDY?
The study procedures and process will vary depending on the type of clinical trial you participate in. Before you begin a study, the process and all procedures for that study will be explained to you. Throughout the study, the Study Coordinator and the Principal Investigator will assist you and can answer any questions you have. They will check your health at the beginning of the trial, give you specific instructions for participating in the trial, monitor you carefully during the trial, and stay in touch with you after the study.
• Some clinical trials involve more tests and doctor visits than you would normally have for your illness or condition. Your participation will be most successful if you carefully follow all instructions, you are given and stay in contact with the research staff.
WHAT ARE THE RISKS OF PARTICIPATING IN A CLINICAL TRIAL?
Most all investigative treatments can cause side effects and other health risks. Side effects and health risks vary from patient to patient. The number of side effects, if any, you experience will depend on the type of treatment being studied and your medical condition.
Before you agree to participate in a study, it is important that you know what side effects may occur and, as much as possible, what unknown side effects or risks may occur. This information will be covered thoroughly during the informed consent process before you enroll.
WHAT IS AN ADVERSE EVENT?
The term adverse event, as used in the context of clinical research, means any untoward medical occurrence in a patient administered a pharmaceutical product which does not necessarily have to have causal relationship with this treatment. Adverse events can be a symptom (e.g., a headache), a finding during a physical exam (e.g., elevated blood pressure), a syndrome or disease (e.g., “flu syndrome” or meningitis), or an abnormal laboratory value.
WILL I GET PAID FOR PARTICIPATING IN A RESEARCH STUDY?
You will usually be paid for your time and travel while participating in a clinical study. Surgery, medical exams, and medical procedures may also be performed at no cost to you depending on the type of study. If a study requires you to stay at a research facility for any length of time, you may also receive meals or snacks.
Meet Our Team
Administrative
Founder & CEO
Clinical Site Manager
Quality Assurance
Principal Investigators
Internal Medicine
Pediatrician
Gynecologist & Obstetrics
General Practice
Dermatology
Psychiatric
Neurology
Sub-Investigators
ARNP-FNP
Coordinators
Nurse Coordinators
CRCC
Assistant Coordinators
EDC Specialist
Phlebotomist
Pharmacist
Contact Us
Phone: 786-667-1617
Fax: 786-539-3073
Mail: info@empireclinicaltrials.com
Location: 890 SW 87th St, Suite 10, Miami, Florida,33174
426 Ridge St , Kissimmee,Florida,34744
923 W 29 St , Miami ,Florida,33012
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