Comité de Ética en Investigación del Hospital SMIQ
Copyright 2024
Science handled
by experts
We are a research center dedicated to the conduct of clinical studies, such as the development of pharmaceutical compounds, biotechnology products and medical devices.
medical
research center
We want to be a reference for the present and a legacy for future generations.
We have a wide network of professional and certified researchers, as well as comprehensive
facilities that allow us to hospitalize and monitor our patients, always prioritizing their safety and well-being.
We strive not only to be at the forefront of clinical research, but also to maintain ethical standards and continuous quality improvement.
About clinical
research
Clinical research is the vital process in which experts study new medical treatments and therapies to improve patient care.
It involves careful, ethical human testing to ensure the efficacy and safety of medical innovations, leading the way for advances that benefit global health.
Our services
Patient care
Proper follow-up and monitoring of patients in our medical center.
PNO Manuals
We have procedure manuals at the different levels of each clinical investigation.
.
Rooms
For the stay of patients, in charge of personnel trained in GCP.
Database
Large database of patients with different pathologies from private practice and public institutions.
.
Call center
For the follow-up of patients to ensure their safety during and after participating in the protocols.
Recruitment
Support to other centers to achieve their recruitment goals.
Experience, our greatest ally
We have developed methods and technology in different areas of study to keep moving forward.
PHASE II
Dermatology
Urticaria
Gastroentrology
NASH, CUCI, Chron, GERD
Infectology
Vaccines
Vaccines
Respiratory syncytial virus pediatrics, geriatrics
PHASE III
Cardiology
Hiercholesterolemia, A FIB, CHF
Dermatology
Psoriasis, Atopic Dermatitis, Dermatitis
Infectology
Diseases vaccines
Nephrology
Focal Segmental Glomerulosclerosis, Nephritis, Polycystic Kidney Disease
Neurology
ALS, Acromegaly, AHD, MS, MS, Multiple Sclerosis
Pneumology
Asthma Pulmonary hypertension, COPD
Rheumatology
Lupus, Rheumatoid arthritis, ALS
Registries
Dermatology and cardiology
Dentistry
Pain treatment
Oncology
Prostate, Breast, Small Cell Lung, Melanoma, Pancreas, Recurrent Cervical Cancer
PHASE IV
Allergology, pediatrics
APLV
Gastroenterology
Amoebiasis treatment
Internal medicine
Herpes zoster, medicines, pain medicine
Some of our sponsors and partners
All the procedures we carry out as part of
our protocols comply with the highest
national and international requirements,
also they are guided and evaluated by our
Ethics and Biosafety Committees.
OUR COMMITTEES
Its mission is to ensure that health research complies with ethical principles and requirements to protect the rights, dignity, safety and general welfare of research subjects and other persons involved in the projects.
research ethics
committee
Our main responsibilities
1
Evaluate
2
Approve
3
Follow up
We have two committees
Approved by CONBIOÉTICA
Registration number:
CONBIOÉTICA-22-CEI-003-20171130
Approved by COFEPRIS
Registration number:
19 CI 22 014 033
For us, it is essential that our work be at the service of individuals and respect their dignity. It is therefore important that ethics and research committees guide their activities and assess them in the light of certain principles, values and standards.
Keep in touch
FAQ'S
Clinical research is scientific research that involves people. Scientists do it to learn more about diseases, as well as to look at new medical treatments or combinations of treatments that doctors already use. The goal is to find new and better treatments that help patients.
Some reasons to participate in clinical research are: to help learn about a disease, to help find new treatments, to receive a treatment that is not yet available to the public, or to receive a new treatment because the usual treatment is not working well.
Clinical research often involves medical treatments. But it is not the same as a standard medical treatment for a disease or condition. Scientists do research to learn and possibly improve treatment for all children in the future.
Many people work together to make sure that scientists conduct clinical research safely and correctly. A group called an Institutional Review Board reviews each new clinical research study at a hospital or medical school before the study begins. The Institutional Review Board, or IRB, is a group of scientists, doctors, other health care professionals and people from the community.
You may receive a new treatment for a disease before it is available to everyone else, you play a more active role in your own health care. As part of your treatment, researchers may provide you with more frequent medical care and health checkups. You may have the opportunity to help others get better treatment for their health problems in the future, as well as information about support groups and available resources.
Science handled
by experts
We are a research center dedicated to the conduct of clinical studies, such as the development of pharmaceutical compounds, biotechnology products and medical devices.
medical
research center
We want to be
a reference for the
present and a legacy
for future
generations.
We have a wide network of professional and certified researchers, as well as comprehensive facilities that allow us to hospitalize and monitor our patients, always prioritizing their safety and well-being.
We strive not only to be at the forefront of clinical research, but also to maintain ethical standards and continuous quality improvement.
About clinical research
Clinical research is the vital process in which experts study new medical treatments and therapies to improve patient care.
It involves careful, ethical human testing to ensure the efficacy and safety of medical innovations, leading the way for advances that benefit global health.
Our services
Patient care
Proper follow-up and monitoring of patients in our medical center.
PNO Manuals
We have procedure manuals at the different levels of each clinical investigation.
Rooms
For the stay of patients, in charge of personnel trained in GCP.
Database
Large database of patients with different pathologies from private practice and public institutions.
Call center
For the follow-up of patients to ensure their safety during and after participating in the protocols.
Recruitment
Support to other centers to achieve their recruitment goals.
Experience,
our greatest ally
We have developed methods and technology in different areas of study to keep moving forward.
Phase II
Dermatology
Urticaria
Gastroentrology
NASH, CUCI, Chron, GERD
Infectology
Vaccines
Vaccines
Respiratory syncytial virus pediatrics, geriatrics
Phase III
Cardiology
Hiercholesterolemia, A FIB, CHF
Dermatology
Psoriasis, Atopic Dermatitis, Dermatitis
Infectology
Diseases vaccines
Nephrology
Focal Segmental Glomerulosclerosis, Nephritis, Polycystic Kidney
Disease
Neurology
ALS, Acromegaly, AHD, MS, MS, Multiple Sclerosis
Pneumology
Asthma Pulmonary hypertension, COPD
Rheumatology
Lupus, Rheumatoid arthritis, ALS
Registries
Dermatology and cardiology
Dentistry
Pain treatment
Oncology
Prostate, Breast, Small Cell Lung, Melanoma, Pancreas,
Recurrent Cervical Cancer
Phase IV
Allergology, pediatrics
APLV
Gastroenterology
Amoebiasis treatment
Internal medicine
Herpes zoster, medicines, pain medicine
Some of our
sponsors and
partners
All the procedures
we carry out as part of
our protocols comply with the highest national and
international requirements,
also they are guided and
evaluated by our Ethics and Biosafety
Committees.
OUR
COMMITTEES
Its mission is to ensure that health research complies with ethical principles and requirements to protect the rights, dignity, safety and general welfare of research subjects and other persons involved in the projects.
research ethics
committee
Our main
responsibilities
1
Evaluate
2
Approve
3
Follow up
clinical studies
For us, it is essential that our work be at the service of individuals and respect their dignity. It is therefore important that ethics and research committees guide their activities and assess them in the light of certain principles, values and standards.
We have
two Committees
Approved por CONBIOÉTICA
Registration number:
CONBIOÉTICA-22-CEI-003-20171130
Approved por COFEPRIS
Registration Número:
19 CI 22 014 033
Keep
in touch
For more information about our committees and research centers, please contact us:
FAQ'S
Clinical research is scientific research that involves people. Scientists do it to learn more about diseases, as well as to look at new medical treatments or combinations of treatments that doctors already use. The goal is to find new and better treatments that help patients.
Some reasons to participate in clinical research are: to help learn about a disease, to help find new treatments, to receive a treatment that is not yet available to the public, or to receive a new treatment because the usual treatment is not working well.
Clinical research often involves medical treatments. But it is not the same as a standard medical treatment for a disease or condition. Scientists do research to learn and possibly improve treatment for all children in the future.
Many people work together to make sure that scientists conduct clinical research safely and correctly. A group called an Institutional Review Board reviews each new clinical research study at a hospital or medical school before the study begins. The Institutional Review Board, or IRB, is a group of scientists, doctors, other health care professionals and people from the community.
You may receive a new treatment for a disease before it is available to everyone else, you play a more active role in your own health care. As part of your treatment, researchers may provide you with more frequent medical care and health checkups.
You may have the opportunity to help others get better treatment for their health problems in the future, as well as information about support groups and available resources.