How it Works?
Find out how we contribute to the advancement of medicine and how you can be a part of it.
Meet Inclusion Criteria
Before you can participate in a clinical trial, you must meet certain eligibility criteria that may include factors such as age, gender, type and stage of disease, and medical history.
Informed Consent
Once you are determined to be eligible, you will be provided with detailed information about the study, including potential risks and benefits. This process, known as informed consent, ensures that you fully understand what your participation entails before signing the consent document
Medical Examination and Evaluation
After giving your consent, you will go through a series of medical examinations and assessments to establish a baseline of your health status. These exams help the investigators gain a detailed understanding of your condition before beginning study treatment.
Meet Inclusion Criteria
Before you can participate in a clinical trial, you must meet certain eligibility criteria that may include factors such as age, sex, type and stage of disease, and medical history.
Informed Consent
Once you are determined to be eligible, you will be provided with detailed information about the study, including potential risks and benefits. This process, known as informed consent, ensures that you fully understand what your participation entails before signing the consent document
Medical Examination and Evaluation
After giving your consent, you will go through a series of medical examinations and assessments to establish a baseline of your health status. These exams help the investigators gain a detailed understanding of your condition before beginning study treatment.
Benefits
These are the benefits you will get for participating in our studies
Access to Innovative Treatments
High Quality Medical Care
Compensation for Participation
Contribution to Scientific Progress
Potential Patient Pathway
This itinerary ensures an organized and safe experience for patients participating in clinical trials.
Initial Consultation and Evaluation
Schedule an Appointment: The patient contacts the clinic to schedule an initial appointment through the website, phone call or in-person visit.
Interview and Evaluation: The patient attends the initial appointment where a detailed medical history interview is conducted and preliminary evaluations are performed to determine eligibility for clinical trials.
Selection and Informed Consent
Review of Available Studies: Based on the initial assessment, the most appropriate clinical studies for the patient are identified.
Information Session: The patient receives a detailed explanation of the studies, including objectives, procedures, benefits and risks.
Signing of Informed Consent: The patient signs the informed consent form to confirm participation.
Active Study Participation
Study Assignment: The patient is assigned to one of the clinical studies according to his/her profile and needs.
Visits and Follow-up: The patient makes regular visits to the clinic for follow-up, where tests, treatments and monitoring are performed according to the study protocol.
Continuous Communication: The patient maintains constant communication with the research team to resolve any doubts or report side effects.
Final Evaluation and Results
Closure Evaluation: At the end of the study, the patient attends a final evaluation to review the results and his or her health status.
Results Report: The research team provides a detailed report of the findings and, if necessary, recommendations for future care.
Post-Study Follow-up: The patient receives additional follow-up if necessary to ensure his or her well-being after the study.
Join our clinical studies and contribute to the advancement of medicine!
Participating in our trials not only gives you access to innovative treatments and cutting-edge medical care, but also helps improve global health.