At eCTD Submit, trust and reliability form the foundation of our client relationships. These core operational qualities, combined with our regulatory expertise, drive the customer relationships that we build. At eCTD Submit we combine these qualities to offer seamless eCTD publishing services for life sciences organizations of all sizes. Our proven track record has made us a trusted partner for clients who depend on precision and accountability in their regulatory submissions. Many of our long-term clients continue to rely on our services, even as they transition to new organizations—a testament to the value we deliver.
As example, consider one of our long-time clients: an accomplished pharmaceutical CMO who turned to eCTD Submit for support with a U.S. IND submission. Our working relationship began many years ago when this client needed to submit a U.S. IND and sought support from experts with proven FDA submission expertise.
At the time the client was assessing multiple vendors but chose eCTD Submit for our promise: no delays, none of the typical submission headaches often experienced with other publishers.
The result? As expected, a seamless submission, completed without a hitch. Although at that time eCTD Submit was a new company, the team already had a long-proven track record in regulatory publishing.
When our client moved on to a new role at a new organization, they brought along their working relationship with eCTD Submit. Since then, eCTD Submit has consistently exceeded all their submission needs and expectations, with multiple successful U.S. IND submissions in rapid succession and well ahead of the planned submission date.
Where eCTD Submission Flexibility and Accountability Serve Your Infrastructure
For small or emerging organizations, limited internal resources can make regulatory submission publishing a challenge. Outsourcing to a large vendor can be problematic if the vendor can’t deliver responsiveness and adaptability—necessary for any small team that depends on quick, adaptive, and reliable partners. Large or small, life sciences organizations need an eCTD publisher who can be entrusted with critical responsibilities without risking submission failure.
And for overseas clients requiring expert US agent services, accessibility and reliability is essential—a thorough understanding of FDA regulations is only useful if the publisher can also be counted upon to prioritize efficient communication and adaptive flexibility during the eCTD submission process.
Accessibility and Reliability: The eCTD Submit Standard
Every client we serve benefits from:
- Direct communication with our leadership to quickly address any issues.
- Unfettered access to our experienced eCTD submission team.
- Consistent collaboration and consensus decision making to ensure alignment and success.
This powerful combination of accessibility, regulatory expertise, and superior eCTD software form an unrivaled eCTD submission experience. For our overseas clients, eCTD Submit remains a preferred provider of US agent services and regulatory expertise. Our deep knowledge combined with a well-defined submission process ensures compliance oversight and the prevention of regulatory missteps, handoff errors, and miscommunications that occur all too often with unintegrated providers of eCTD submission and U.S. agent services.
Partner with eCTD Submit Today
We’ve been performing eCTD submissions since the inception of the eCTD itself.
Reach out today to see how a responsive, flexible, and accountable eCTD publishing provider can elevate your regulatory submissions.
