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Ep. 10: Regulatory Affairs - Connecting all the Dots with Fernanda Manhães

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Content provided by The Pharmadelic Experience. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by The Pharmadelic Experience or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ro.player.fm/legal.

Fernanda holds a degree of Industrial Pharmacy from the Universidade Federal Fluminense in Brazil, including a one year exchange in the University of Claude Bernard – Lyon 1 in France. Graduated with a work experience in Research Lab, Hospital Pharmacy and Regulatory Affairs in the pharma industry, she decided to jump back to Europe to follow her career as a Regulatory Affairs Specialist in Italy. After going deep in the Technology topic related to Regulatory Affairs in Germany, she went back to the pharma industry in Switzerland as Regulatory Affairs Manager, focusing on implementing strategy of orphan drugs registration in US and Swiss markets.

  continue reading

15 episoade

Artwork
iconDistribuie
 
Manage episode 327377028 series 3090907
Content provided by The Pharmadelic Experience. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by The Pharmadelic Experience or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ro.player.fm/legal.

Fernanda holds a degree of Industrial Pharmacy from the Universidade Federal Fluminense in Brazil, including a one year exchange in the University of Claude Bernard – Lyon 1 in France. Graduated with a work experience in Research Lab, Hospital Pharmacy and Regulatory Affairs in the pharma industry, she decided to jump back to Europe to follow her career as a Regulatory Affairs Specialist in Italy. After going deep in the Technology topic related to Regulatory Affairs in Germany, she went back to the pharma industry in Switzerland as Regulatory Affairs Manager, focusing on implementing strategy of orphan drugs registration in US and Swiss markets.

  continue reading

15 episoade

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