Carolina Ureña personal email
- Valid
Carolina Ureña is a Gerente de país at Adiuvo-Droguería Europea. She possess expertise in regulatory affairs, regulatory submissions, pharmaceutical industry, gmp, gcp and 12 more skills. She is proficient in English.
Adiuvo-Droguería Europea
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Gerente De PaísAdiuvo-Droguería Europea Oct 2021 - PresentEscazú, San Jose, Costa Rica
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Senior Regulatory Affairs SpecialistAdiuvo-Droguería Europea Jan 2021 - Feb 2022
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Regulatory Affairs CoordinatorIndepend Aug 2017 - Jan 2021Consultorías de asuntos regulatorios, manejo de cartera completa de productos farmacéuticos (medicamentos que requieren demostrar bioequivalencia, dispositivos médicos, etc). Experiencia en traducciones no oficiales de documentos médicos y farmacéuticos, incluyendo estudios clínicos, dossiers y documentos técnicos.
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Regulatory Affairs CoordinatorBioplus Care Apr 2016 - Jul 2017
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Regulatory Affairs AssociateEli Lilly And Company Dec 2014 - Apr 2016
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Coordinadora De Asuntos Regulatorios/ Regulatory Affairs CoordinatorNutrimed Feb 2012 - Nov 2014Nutrimed
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Internado Farmacia Industrial/Asuntos RegulatoriosRoche Pharmaceuticals Jun 2011 - Feb 2012Tesis: Quality Risk Management/Análisis de Riesgos de Calidad -
Profesora QuímicaUcimed Jul 2010 - Jul 2011
Carolina Ureña Skills
Carolina Ureña Education Details
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Pharmaceutical Marketing -
UcimedPharmacy -
Internatinal Canadian High SchoolBachillerato
Frequently Asked Questions about Carolina Ureña
What company does Carolina Ureña work for?
Carolina Ureña works for Adiuvo-Droguería Europea
What is Carolina Ureña's role at the current company?
Carolina Ureña's current role is Gerente de país.
What is Carolina Ureña's email address?
Carolina Ureña's email address is ur****@****ail.com
What schools did Carolina Ureña attend?
Carolina Ureña attended Iebs Business School, Ucimed, Internatinal Canadian High School.
What skills is Carolina Ureña known for?
Carolina Ureña has skills like Regulatory Affairs, Regulatory Submissions, Pharmaceutical Industry, Gmp, Gcp, Ich Gcp, Pharmaceutics, Pharmacovigilance, Clinical Development, Validation, Market Access, Clinical Trials.
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