Personal Information
Entreprise/Lieu de travail
Valencia Area, Spain, Valencia Spain
Secteur d’activité
Medical / Health Care / Pharmaceuticals
Site Web
http://www.revipharm.es/
À propos
Professional Summary
- Professional with 10 years of experience in the Pharmaceutical Industry and other Healthcare Companies, mainly in Regulatory Affairs and Pharmacovigilance
- Experience in regulatory affairs (CTD, NEES), drug safety (CIOMS, P/DSUR), data management, medical writing (SmPC, PIL)
- Very knowledgeable about ICH guidelines, EU directives and regulations in Regulatory Affairs and Pharmacovigilance
- Committed to quality, process improvement and regulatory compliance
- Experience in medical devices, cosmetics and OTC products
Self motivated with excellent leadership, presentation, training, supervisory, and organizational skills.
Interests in travelling, music, digital ph...
Mots-clés
medicamentos de uso humano
asusntos regulatorios
sistema maestro de farmacovigilancia
ips
persona responsable de farmacovigilancia
farmacovigilancia
psur
psmf
local and european qppv
training
quality system
regulatory affairs
pharmacovigilance
Tout plus
Présentations
(2)J’aime
(3)An Introduction to the Pharmacovigilance System Master File
TransPerfect Trial Interactive
•
il y a 10 ans
How to build a global passion brand: Insights from the 2013 Social@Ogilvy Brand Advocacy Study
Ogilvy Consulting
•
il y a 10 ans
How to sell - some tips from Ogilvy
Synergia
•
il y a 13 ans
Personal Information
Entreprise/Lieu de travail
Valencia Area, Spain, Valencia Spain
Secteur d’activité
Medical / Health Care / Pharmaceuticals
Site Web
http://www.revipharm.es/
À propos
Professional Summary
- Professional with 10 years of experience in the Pharmaceutical Industry and other Healthcare Companies, mainly in Regulatory Affairs and Pharmacovigilance
- Experience in regulatory affairs (CTD, NEES), drug safety (CIOMS, P/DSUR), data management, medical writing (SmPC, PIL)
- Very knowledgeable about ICH guidelines, EU directives and regulations in Regulatory Affairs and Pharmacovigilance
- Committed to quality, process improvement and regulatory compliance
- Experience in medical devices, cosmetics and OTC products
Self motivated with excellent leadership, presentation, training, supervisory, and organizational skills.
Interests in travelling, music, digital ph...
Mots-clés
medicamentos de uso humano
asusntos regulatorios
sistema maestro de farmacovigilancia
ips
persona responsable de farmacovigilancia
farmacovigilancia
psur
psmf
local and european qppv
training
quality system
regulatory affairs
pharmacovigilance
Tout plus