Medfiles

💡 Are you making the most of health claims in your food marketing? Join our free webinar on 10 November to learn how to use existing authorised EU health claims and what opportunities a new health claim application could offer. Health claims can help companies communicate the benefits of foods and food ingredients to consumers. However, their use is subject to specific EU requirements, and suitable authorised claims are not always available. I'll discuss the use of existing health claims, while my Medfiles colleagues will explain what is needed to obtain authorisation for a new claim. 📅 10 November | 14:00–14:45 EET + recording 👉 Register for free: https://lnkd.in/dCgyQEjz #healthclaims #foodregulatoryaffairs #foodmarketing

📋Does your food ingredient have scientifically demonstrated health benefits, but no authorised health claim you can use in EU marketing? Join our free webinar on 10 November to learn what scientific evidence is needed to support a health claim application and why early regulatory and strategic planning matters. Promising research is only the starting point. Identifying evidence gaps and understanding the regulatory expectations early can help you build a stronger and more focused application strategy. Together with my experienced Medfiles colleagues, I'll discuss the EU health claim authorisation process, scientific substantiation and key considerations when considering an application. 📅 10 November | 14:00–14:45 EET + recording 👉 Register for free: https://lnkd.in/dxaBSBzK #healthclaims #foodregulatoryaffairs #EFSA

What does it take to get a new health claim authorised in the EU? ✅ Join our free webinar on 10 November to learn about the scientific evidence, regulatory requirements and documentation needed for an EU health claim application. Preparing a successful application requires careful planning, from evaluating existing scientific evidence to identifying potential data gaps and meeting EFSAs requirements.Ill be sharing practical insights into the application process together with my Medfiles colleagues, who will also discuss clinical studies and the use of authorised health claims. 📅 10 November | 14:00–14:45 EET + recording 👉 Register for free: https://lnkd.in/d-a4GJsw #healthclaims #foodregulatoryaffairs #EFSA

A newsletter on animal health is now out! 📩🐾 Topics include: 🔹New EU veterinary GMP regulations and quality system expectations 🔹Upcoming revision of the VGVP Signal Management Module 🔹Key trends affecting the animal health industry in 2026 🔹Recent feed legislation and regulatory developments Read below and subscribe to Medfiles Pulse for more expert insights. ⬇️ #veterinarymedicine #animalfeed #animalhealth #medfilespulse

In our latest article, we share four real-life examples of how pharmaceutical companies have outsourced local regulatory affairs activities in the Nordic and Baltic markets, from market entry preparations to ongoing post-approval support and Responsible Pharmacist services in Finland. The common denominator? Flexible access to local regulatory expertise that helps companies stay compliant while allowing internal teams to focus on other strategic priorities. If you are evaluating your local regulatory affairs setup, planning market expansion, or looking for additional regulatory expertise in the Nordics or Baltics, feel free to reach out. We'd be happy to discuss your situation and explore how we could support your team. Read more in the article below. 👇 https://lnkd.in/dXk_y9KN And a small bonus: When you partner with Medfiles, you'll get to work with experts like Mari Lindevall, who authored this article and represents the kind of practical, solution-oriented regulatory expertise that our clients value every day. 😊

Meet Anna Lyra, our Senior CRA and Medical Writer. 💎 With 20+ years of experience in clinical research and scientific writing, Anna supports clients throughout the study lifecycle, from planning and monitoring to documentation and final reporting. One of Anna's strengths is her ability to combine scientific expertise with a practical understanding of how studies are planned, conducted, documented and reported in the real world. Her experience spans medicinal products, medical devices and food studies, as well as roles in research, monitoring, project management and medical writing. Read more about Anna's work and expertise ➡️ https://lnkd.in/eK6xVNeg #clinicalresearch #clinicaltrials #medicalwriting #workatmedfiles