top of page
Paciente felíz
PATIENTS

If you are interested in learning more about patient participation in clinical protocols, please take a moment to fill out a brief confidential pre-registration questionnaire. Take the first step, there may be a protocol in which you or someone you know may qualify.

 

NOTE: You will not be included in any Clinical Trial without your consent. Remember that participation in a research protocol is voluntary :).

I am interested

What is Clinical
Research?

National and international regulations require that each drug undergoes a series of clinical research before it is approved by regulatory agencies, such as the WHO, FDA and COFEPRIS; it must also be approved by a Research Ethics Committee, which will ensure that the integrity of the patients participating in such research is safeguarded, and that each research process is in accordance with the guidelines issued by it. 

Research Protocols are of utmost importance for the advancement of medicine, making these drugs available to the market.

​

In Mediadvance Clinical, it is our mission to play an integral role in these medical advancement processes.

​

Médico y paciente
Que es la investigción

Benefits of participating in a
Clinical Trial

NOTE: Participation in a Research Protocol is a completely voluntary decision on the part of the patient. No coercion or pressure will be applied by Mediadvance Clinical staff to the patient to participate in the study. Likewise, no patient will be administered study medication if they choose NOT to participate in the Research Protocol.

1.

 

​

​

3.

 

​

​

4.

2.

You will help in the development of new medical treatments for people with different diseases.

 

You will receive specialized medical care at no cost.

 

If you are eligible, you will receive the study medication at no cost

 

You will receive a variety of medical services at no cost, such as laboratory tests, medical consultations, imaging, electrocardiograms, etc.

bottom of page