Luminance Webinar – Launching Medicinal Products in Europe
Luminance conducted a tailored webinar for life science professionals in Asia and North America preparing to launch pharmaceutical products in the European Union. The event provided a focused yet thorough exploration of the essential requirements for a successful market entry, equipping attendees with actionable insights and strategic guidance.
The session, led by Luminance specialists including Joanna Hanley (Head Quality Assurance), Philipp Ansorge (Head Pharmacovigilance) , Ben Stockham (Director Regulatory Affairs) and external speakers Rute Fernandes (Pharma Executive and Board Member), Thomas P. Wenk (Hoffmann & Partner AG) and Oliver Wunderle(Hoffmann & Partner AG), addressed the multifaceted challenges of launching medicinal products in Europe. Participants benefited from expert advice across key operational domains, ensuring they are well positioned for compliant, cost-effective, and commercially viable product launches throughout the region. Key topics discussed included a roadmap of EU regulatory requirements, with best practices for dossier submission, product approval, and lifecycle management. The webinar also covered proven strategies for maintaining Good Manufacturing Practice (GMP) compliance and safeguarding supply chain integrity across all EU member states.
Basel, Switzerland | 09.09.2025