Pharmacovigilance

Reaction Report

Do you have any reaction?

At ULSA TECH, we are committed to complying with the highest standards and guaranteeing both the therapeutic effectiveness and the safety of all our products through research, bioequivalence studies and strict quality control; However, any medication, even when administered correctly (under medical prescription), in the appropriate concentration and dosage, can present adverse effects caused by the reaction of each organism to the medication (allergic reactions), interaction with other medications, and other variables not included in the prescribing information.

The responsibility of ULSA TECH, as a Pharmaceutical Laboratory, must go beyond the manufacture and distribution of medicines.

Therefore, as a company committed to complying with the health authority in the implementation of Pharmacovigilance, based on NOM-220-SSA1-2016, it is through a Pharmacovigilance Unit recognized by the Federal Commission for the Protection against Health Risks (COFEPRIS) and made up of health professionals and technical staff, we oversee recording adverse reactions to drugs and new therapeutic applications, to monitor the safety and efficiency of the drugs we make.

 

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