Planning a Clinical Trial? Don’t Miss This IND/CTA Webinar on Sep 3rd
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?