For customers outside of Japan
| Regulatory Consultation | |
|---|---|
| Regulatory Authorities | Protocol Development |
| Conduct Clinical Trial | |
|---|---|
| * KOL communication * Feasibility |
Optimized team |
| NDA Submission-Launch | |
|---|---|
| Inquiries / Inspection | Post Marketing Service |
Collaboration with a strong partner companyallows us to provide services across APAC countries and USA.
We assign specialists who are deeply familiar with the local regulations and medical environment in each of the countries in which we operate.
Development strategies are critical to the success of any project, and we can help you develop them with our high level of expertise.
A proper timeline is set for the entire project, and the project manager works in harmony with the client, site, and vendors to execute the project.
Our track record, cultivated through years of experience, includes experience in a variety of Therapeutic Areas. We propose specialists who have the necessary experience for each project.
Our project manager will always be close to You, our customer, and will guide you appropriately to your desired goal.
From single-service to full-service clinical development and PMS, we are flexible enough to respond to your changing needs.
As a company that plays an important part in the development of healthcare, EPS Group puts patients first and practices highly transparent corporate activities rooted in a high level of ethics.
For the past 30 years, we have supported clinical development in Japan as a leader in the CRO industry. We will continue to provide innovative output with the know-how of our many group companies and more than 6,000 employees.
By setting up a proper communication plan and Issue Escalation plan, any problems that occur will be quickly shared with the team. Problems are then solved by the right people on the team.
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