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Clinical Studies

What is a Clinical Study?

This is a research study in which people participate voluntarily to evaluate the safety and efficacy of new medications and/or treatments. It is controlled and monitored by an Ethics Committee and by ANMAT (National Administration of Drugs, Food and Medical Technology), which guarantees the protection of participants. Participation is free, and participants can withdraw at any time.

What is it like to participate in a Clinical Study?

1

Initial Assessment

The medical team reviews the medical history and determines if the person meets the study criteria.
2

Informed Consent

Complete information about the study is provided, including objectives, procedures, possible risks and benefits, so that the person can freely decide whether to participate.
3

Start of the Study

The visits and procedures established in the study protocol are carried out.
4

Medical follow-up

Throughout the study, the participant receives clinical monitoring and follow-up from the research team.
5

Completion of the Study

A final evaluation is carried out as established in the protocol.

What does participating in a Clinical Study involve?

  • Access to specialized medical follow-up throughout the study
  • More frequent clinical check-ups than in usual practice
  • Contribution to the development of new medicines and treatments
  • Participation in a process regulated under strict safety and ethical standards, established by national/international bodies. (ANMAT / EMA)

Participation does not replace regular medical care, and if you have any concerns, it is recommended that you consult your primary care physician.

Frequently Asked Questions:

Who can participate?

Each study has specific inclusion and exclusion criteria (such as age, diagnosis, or medical history). The team evaluates each case to determine if a person is eligible to participate.

Yes. Participation is completely voluntary and the patient can leave the study at any time, without this affecting their usual medical care.
It is a process through which all the information about the study (objectives, procedures, possible risks and benefits) is provided so that the person can decide to participate freely and consciously.
All studies are conducted under strict Good Clinical Practice (GCP) standards and have the approval of local and provincial Ethics Committees, as well as national and international regulatory authorities, such as ANMAT (National Administration of Drugs, Food and Medical Technology) and the EMA (European Medicines Agency).
Participation in a clinical study is free for the patient.

The Ethics Committee reviews and oversees studies to protect the rights, safety, and integrity of participants.

You can contact our team to learn about the available studies. We will evaluate your case individually according to the criteria of each protocol.

More information for patients