Daniel Dantas

Daniel Dantas is a highly experienced professional in the field of Quality and Regulatory Affairs, currently serving as the Technical Responsible and Quality and Regulatory Affairs Manager at EFFIK since April 2017, with responsibilities for quality management and regulatory activities in Switzerland. Prior experience includes serving as EU Regulatory Affairs Manager at Vifor Pharma/OM Pharma, where oversight included regulatory strategy and medicinal product registrations across the EU, Switzerland, and the CIS region. Previous roles also include Regulatory Affairs Specialist at Novartis Consumer Health and Regulatory Affairs Officer at Bayer Santé Familiale, where Daniel was involved in various regulatory submissions, product updates, and compliance activities. Daniel holds a Master's degree in Pharmacology and Pharmaco-chemistry from Université Louis Pasteur (Strasbourg I).