How it work?
How to Participate?
Joining a clinical study at FelicidadMed Research is easy and safe. If you are interested, you can follow these steps:
Initial Contact
Contact us through our online form or call our offices.
Preliminary Evaluation
Our team will evaluate your eligibility for the study.
Informed Consent
You will receive all the necessary information to make an informed decision.
Active Participation
You will be part of a team committed to your well-being and to the advancement of medical science.
Benefits
Participating in clinical trials with Felicidad Med Research offers numerous benefits to both patients and the medical community at large. Participants have the opportunity to access innovative and advanced treatments before they become commercially available. In addition, they receive high quality medical care from a team of dedicated professionals, ensuring continuous follow-up and care throughout the study.
Access to Innovative Treatments
By participating in our clinical trials, patients have the opportunity to receive advanced treatments and new drugs before they are available on the market.
High Quality Medical Care
Participants receive detailed and personalized follow-up by a team of highly qualified health professionals, ensuring optimal care throughout the study.
Contribution to Medical Advancement
Your participation helps improve future treatments and therapies, benefiting thousands of people who may suffer from similar conditions in the future.
Time and Travel Compensation
We offer financial compensation to cover time and travel expenses, recognizing the effort and dedication of our participants.
Potential Patient Pathway
Identification and Initial Contact
The interested patient can find information about available clinical studies through our website, social networks or medical references. Initial contact with the Felicidad Medical Research team to express interest and obtain preliminary information.
Eligibility Evaluation
The research team reviews the patient's medical history and performs a preliminary assessment to determine if the patient meets the study's inclusion criteria. Performing tests and examinations necessary to confirm the patient's eligibility.
Informed Consent
The patient receives a detailed explanation of the study, including potential risks and benefits. Signing of the informed consent form, ensuring that the patient fully understands the study and agrees to participate voluntarily.
Study Enrollment
The patient is officially enrolled in the clinical study. Scheduling of visits and procedures according to the study protocol.
Active Participation and Follow-up
Patient attends all scheduled visits and follows study protocol instructions. Receipt of treatment and regular monitoring by the medical team. Recording of data and observations necessary for the study.
Completion of the Study and Results
At the conclusion of the study, the patient is informed of the results and any relevant findings. Final evaluation and recommendations for continued care or future treatments.
