Join us in this episode as we delve into the complex world of medicinal product labelling—a cornerstone of patient safety and regulatory compliance. We’ll explore:
- Evolving EU requirements: product names, active substances, strengths, and routes of administration;
- The impact of 2D QR codes and Braille: innovations for inclusive and accessible communication;
- The regulatory evolution of multilingual labelling: how to manage multi-language content while maintaining clarity and compliance;
- Operational challenges and practical solutions: from label design to approval, with a focus on version control and content consistency.
This episode is tailored for regulatory affairs, quality, and packaging professionals. Expect real-life examples, best practices, and key insights to navigate complexity efficiently—reducing risk and speeding up time to market.
Why listen:
- Stay up to date with evolving regulations and global trends.
- Gain actionable strategies to streamline internal processes—from creation to approval.
- Strengthen product quality and safety, a key differentiator in a competitive market.
Get ready to decode
medicinal labelling like never before: where technology, regulation, and accessibility come together to ensure that every patient receives the right information, the right way.
