Need to move faster from preclinical to first-in-human? CMC timelines for IND/CTA submissions can make or break a development plan. In this webinar, our CMC and regulatory experts will share how to avoid common bottlenecks and build submission strategies aligned with both FDA and EMA expectations.
o What typically causes delays when filing in both the US and EU?
o How can early CMC planning shorten your submission timeline?
o What support can you tap into from regulators today?
You’ll hear real-world case studies, agency insights, and time-saving tips to help you confidently move your clinical program forward.
Webinar Details
o Date: September 3, 2025
o Time: 10 am EDT (NA) / 3 pm BST (UK) / 4 pm CEST (EU-Central)
Reserve Your Spot Now!