Webinar: Regulatory Outlook 2026: The Road Ahead for eCTD, IDMP & ePI

The regulatory landscape never stands still – and 2026 will bring significant changes for eCTD, IDMP, and ePI requirements across the globe. In this complimentary live webinar, we’ll look ahead together and explore what’s coming, what it means for you, and how to navigate the road ahead with confidence.

Your guides Priya Krishnan, Business Consultant, and Frank Dickert, Senior Business Consultant – both from our Regulatory Competence Center – will share practical insights and valuable information on what to expect for the regulatory year 2026. With years of hands-on experience in global submissions, they have a lot of knowledge up their sleeve to help you prepare for the next regulatory chapter.

Join this 60‑minute session to find out more about:

• eCTD v4 outlook and other eCTD changes worldwide – from new introductions in Bosnia and Tunisia to updates in Taiwan, China, and the EU
• The latest in IDMP and ePI – what new EU and Swissmedic initiatives mean for your data and processes, and how to ensure readiness
• US FDA and ICH updates – Pharmacovigilance changes and ICH M4Q(R2) - stay compliant and avoid last‑minute surprises!

What you’ll gain:

• A clear, consolidated view of upcoming changes through 2026
• An understanding of how these developments will impact your daily work and long‑term projects
• Recommendations that help to meet deadlines, minimise risks, and stay ahead

Whether you work in the US, Europe, Asia, or across multiple regions, this webinar will equip you with the insight and guidance you need before the new rules take effect.

Register now to save your seat today and join us for a forward‑looking discussion and actionable advice.

Not sure if you can join live? Just register and receive the recording. 

Your Speakers:

	Priya Krishnan Business Consultant
	Frank Dickert Senior Business Consultant