Andres Lopez Velasco

Andres Lopez Velasco

Senior Regulatory Affairs Specialist @ Clever Leaves

About Andres Lopez Velasco

Andres Lopez Velasco is a Senior Regulatory Affairs Specialist with over 12 years of experience in drug regulation and policy. He has specialized knowledge in international legislation for narcotics control and has worked at Clever Leaves in Germany since 2019.

Work at Clever Leaves

Andres Lopez Velasco has been employed at Clever Leaves as a Senior Regulatory Affairs Specialist since 2019. In this role, he focuses on regulatory compliance and policy development related to drug regulation. His position involves navigating complex regulatory landscapes and ensuring adherence to international standards. His experience in this capacity contributes to the company's efforts in the cannabis industry, particularly in Germany.

Education and Expertise

Andres Lopez Velasco holds a Magister en Ciencias - Quimica, specializing in catalisis heterogenea, from Universidad Nacional de Colombia, where he studied from 2005 to 2009. He also earned a degree in Chemistry (Quimico) from the same institution, completing his studies from 2000 to 2005. His academic background provides a strong foundation for his expertise in drug regulation and policy innovation.

Background

Prior to his current role, Andres Lopez Velasco worked at Universidad Nacional de Colombia in various capacities. He served as an Investigador Auxiliar from 2005 to 2007, where he contributed to research initiatives. Additionally, he worked as a Docente Auxiliar from 2006 to 2007, engaging in teaching responsibilities in Bogota DC. These experiences helped shape his understanding of regulatory affairs in the context of academia.

Regulatory Affairs Experience

With over 12 years of experience in drug regulation and policy, Andres Lopez Velasco possesses specialized knowledge in international legislation governing narcotics and psychotropics. His expertise includes innovation in drug policies and the international monitoring and review of drug policy scenarios. This extensive background supports his role in regulatory affairs and enhances his contributions to the field.

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