Erick Maximiliano F. Email and Phone Number

Pharmacovigilance Responsibilities:- Evaluated more than 30 adverse events from various medical departments, determining the seriousness, casualty, and intensity of each.- Entered the data for each case with the appropriate coding into the safety database, successfully notifying regulatory authorities of the event.- Prepared more than 30 safety reports, including corrective or preventive measures, to ensure the safety of the drug and, most importantly, of the patients.Responsibilities in the Mixing Center:- Validated up to 50 medical prescriptions for intravenous mixtures daily, both oncological and nutritional, to ensure they meet established requirements.- Prepared and conditioned the mixtures, ensuring they met appropriate stability requirements, to guarantee a high-quality product for patient administration.Other Responsibilities:- Responsible for dispensing over 100 basic, high specialty, and intravenous medications daily to patients.

-Conducted statistical studies on 4 active principles, which demonstrated that the lab tests made by the manufacturer are equivalent to those made at the local site.-Compiled regulatory documents to prove that the active ingredients comply with Good Manufacturing Practices (GMP). -Prepared an analytical report, which recommended the elimination or reduction in the frequency of certain tests performed on the active principle based on solid statistical and risk analysis evidence,