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We are an authorized third party

We are authorized by COFEPRIS as a Clinical Unit to perform Bioequivalence Trials.

Our Quality Policy:
As a clinical research unit, at the Pharmacological Research Center of the National Cancer Institute (INCan) we are committed to our sponsors, suppliers and other interested parties to conduct clinical studies based on scientific, ethical and regulatory knowledge, with the aim of complying with  the applicable needs and expectations, act with impartiality, ensure the safety and well-being of research subjects, obtain complete clinical data and traceable and reliable biological samples; as well as to collaborate with the sustainability of the Institute and contribute to the generation of effective, safe and quality therapeutic options for patients, supported by a Quality Management System with risk-based thinking and with a focus on the continuous improvement of the processes and quality.

Mission

Design and develop clinical studies aimed at demonstrating the safety, efficacy, bioequivalence and/or biocomparability of innovative, generic or biocomparable drugs; contributing with this, to the generation of new alternatives of treatment for the patients.

Vision

Consolidate as a COFEPRIS authorized third party for clinical bioequivalence and biocomparability studies; as well as being the main cancer pharmacological research center in Mexico, with international reach.

Values

Respect. We carry out all our activities out of deep respect for patients, our clients, the institution to which we belong, our coworkers, providers (internal and external) and human rights.

Integrity. We are committed to generating impartial, quality results in the shortest possible time, in order to support the pharmaceutical industry in generating new treatment alternatives that are safe, effective and of quality for patients.

Passion for Quality. We focus the leadership and commitment of the organization on identifying and understanding the requirements of all interested parties in order to systematically fulfill them through our processes.

Our facilities

At the CIF we have the necessary spaces to carry out phase, bioequivalence and biocomparability studies in healthy volunteers and patients (mainly cancer patients).

Taking samples and signs

Infirmary and emergencies

Volunteer areas

Support areas

Job center

INCan Areas

Taking samples and signs

15 reposet chairs for chemotherapy and sample collection | Sample processing area with controlled access, which has a centrifuge and deep freezer (-70 ° C) | somatometry area

Infirmary and emergencies

Crash area | Medical emergency area | Nursing Center

Volunteer areas

12 rooms with bathroom (single and shared) with a total of 30 beds | Recreation area | Waiting room | dining room | Exclusive bathroom for volunteers and family members

Support areas

Supplies warehouse | Central document archive | Medicine warehouse at room temperature, refrigeration and with red light for photosensitive products | septic area

Job center

Consulting room for exclusive use in research protocols | Area with computer equipment for administrative and quality personnel and clinical coordinators | Staff meeting room | Monitoring area | Exclusive bathrooms for staff | Room for medical staff on call

INCan Areas

Clinical and imaging lab | Mixing center | Emergency area | Immediate attention with service 24 hours a day, 365 days a year | Pharmacovigilance Unit | Management of RPBI

CIF Team

At CIF we have a list of specialists in the pharmaceutical industry and cancer medicine. Know us.

Research Team

Being part of the National Institute of Cancerology (INCan), we work together with researchers from various areas of this Institute.