Name: Britt Vassbotn Kamfjord Title/position: Senior Adviser/Partner Years at Mericon: 18 years Education: M.Sc. in Zoology, Marine Biology Age: 53 years

Tell us about your background and how you ended up at Mericon.

I originally worked as a florist before pursuing a Master’s degree in Zoology and Marine Biology. My fascination with nature and attention to detail led me to regulatory work, where precision and compliance are crucial. After completing my studies, I moved to Brevik and joined Mericon, where I have worked for 18 years. While my role differs from my academic background, my expertise in biology, combined with my passion for structure, language, and accuracy, makes regulatory advisory work an excellent fit.

What is your role at Mericon?

I primarily focus on post-marketing regulatory tasks, supporting clients with marketing authorisations, translations, and compliance with Norwegian and European regulations. My work involves reviewing and editing documents such as product information, pharmacovigilance materials, and educational material. I also ensure that documentation for veterinary medicinal products is correctly adapted to its target audience, whether veterinarians or pet owners, maintaining accuracy in both terminology and dosing instructions.

What does a typical workday look like?

My daily tasks vary, but often include translating and verifying product information, ensuring compliance with national regulations, and assisting clients with local adaptations. One key focus area is updating product information for veterinary medicinal products to align with the latest QRD template, ensuring consistency and regulatory compliance. Additionally, I provide guidance on submitting materials such as Risk Minimization Plans (RMPs) and reviewing printed packaging material to meet national guidelines.

How do you stay updated on regulatory requirements?

Regulatory work requires continuous learning. I stay updated by monitoring developments from the European Medicines Agency (EMA) and the Norwegian Medical Products Agency (NOMA). I also participate in industry meetings and discussions organised by regulatory bodies and professional associations. Within Mericon, we share knowledge across specialist groups, ensuring that we remain well-informed about regulatory changes and best practices.

How do you see regulatory advisory services evolving in the future?

The regulatory landscape is constantly evolving, with increasing harmonisation across Europe. AI and automation will play a greater role in regulatory processes, streamlining workflows and improving efficiency. However, human oversight will remain essential to ensure compliance, accuracy, and risk mitigation. National regulatory adaptations will still be necessary, as local requirements and healthcare standards differ. While AI can assist in translation and documentation, experienced regulatory advisors will still be needed to verify critical details and maintain the high standards required in the pharmaceutical industry.

How does teamwork contribute to solving regulatory challenges?

At Mericon, we work closely within our specialist groups and across different fields to ensure the best outcomes for our clients. Not everyone can stay updated on every aspect of regulations, so collaboration is key. When a task falls outside my expertise, I consult colleagues or leverage our European network, EUDRACON, which provides access to specialised knowledge beyond our in-house capabilities. This collaborative approach allows us to solve complex challenges efficiently and deliver high-quality regulatory support.

What motivates you in your job?

I take great pride in ensuring the accuracy and quality of regulatory texts. Well-structured and grammatically correct documents are essential for patient safety and effective use of medicinal products. Knowing that my work contributes to clear communication in healthcare and compliance with regulations is highly rewarding. Additionally, the daily interactions with clients and colleagues, as well as the positive feedback I receive, keep me motivated and engaged.

What’s the best part of working at Mericon?

The best part is the combination of meaningful collaboration, professional development, and flexibility. I enjoy working with knowledgeable colleagues who are passionate about regulatory excellence. The ability to shape my own tasks and contribute to the company’s growth is also highly fulfilling. As Norway’s oldest active company within drug regulatory affairs, Mericon has built a strong reputation, and I take pride in contributing to its legacy while helping to shape its future.