We are delighted to announce that Billev Pharma East recently participated in the Global Pharmaceutical Regulatory Affairs Summit 2025, held from 21-23 October 2025 at the Hotel Palace Berlin in Berlin, Germany.
Speaking engagements by Katja Pečjak Reven
We are particularly proud that our Head of Regulatory Affairs, Katja Pečjak Reven, M.Sc. Pharm., served as a speaker for two key presentations:
- “Service Update: Product Management Service” in the “Regulatory Information Management & Digital Transformation” stream on 21 October (08:40–09:20).
- “Industry Case Study: Experiences with ePI” in the “Global eSubmissions” stream on 23 October (09:55–10:40).
Why this matters
The Summit is recognised as a premier gathering for regulatory affairs professionals, covering critical topics such as regulatory information management (RIM), data management, digital transformation in regulatory operations, e-submissions, and the implementation of global standards.
By participating as a speaker, Billev Pharma East reaffirmed its commitment to being at the forefront of regulatory innovation and digital readiness in the pharmaceutical industry.
Benefits for our clients and partners
- Thought-leadership and credibility: our contribution as a speaker underlines our expertise in regulatory affairs and digital transformation.
- Access to cutting-edge insights: we bring back the latest learnings and industry trends from the Summit and imbue them into our services.
- Focus on innovation: with sessions on ePI, RIM, cloud submissions and digital transformation, we are well-positioned to support our clients in taking regulatory operations to the next level.
Looking ahead
The knowledge and connections gained at the Global Pharmaceutical Regulatory Affairs Summit 2025 are already being applied by our team as we refine and enhance our service offerings. If you would like to explore how Billev Pharma East can assist you with regulatory information management, digital transformation or e-submission readiness, please don’t hesitate to reach out.
Thank you to all the participants, speakers, and organisers for an engaging and productive event. We look forward to continuing to drive regulatory excellence — together.