Biotechnology doctor. Regulatory affairs and pharmacovigilance expert. Curious learner, eager sharer.
I have over 4 years of experience in pharmacovigilance and drug safety related topics. I worked in the Mexican Competent Authority (COFEPRIS) being a permanent PV expert for the New Molecules Committee (in charge of new IMPs approvals).
I am a PV consultant and regulatory required documents producer.
Safety reporting to CAs, ECs and INV around the world are also included in my experience.
I have over 4 years of experience on regulatory affairs in Mexico. I have worked at the Mexican Competent Authority (COFEPRIS).
Drug marketing related regulatory affairs is one of my expertise areas.