Global Publishing and eCTD Submission Services
Prepare for your next regulatory filing with 6 tips from our experts.
Leverage Pearl Pathways’ regulatory and publishing experts to comply with FDA’s standard eCTD submission format. Our team includes former FDA talent and boasts a 99% on-time delivery rate across all types of product applications. If you are looking to outsource your regulatory publishing activities, Pearl Pathways is ready for your next IND, NDA, ANDA, BLA, or Drug Master File submission. Complete the form below to download the 6 Tips for Successful eCTD Preparation guide.
“Pearl submitted two INDs for us and they were done quickly and without issue. We were very pleased with the work and timeline. Working with Pearl allowed our INDs to get through with only minimal questions from FDA and no major issues.”
– CEO and Founder, Startup biopharma company