All parties benefiting from the services provided by Orjin Clinical Research Solutions are deemed to have accepted these Terms of Use.

Orjin CRS conducts investigational product and equipment procurement, site operations, archiving services, and related support activities within clinical research in accordance with applicable national and international regulations, ICH-GCP guidelines, and the requirements of its Quality Management System.

Users and business partners agree to use all services and information provided solely for lawful and authorized purposes and to comply with applicable laws, regulations, and contractual obligations.

All documents, data, and systems provided by Orjin CRS are confidential. Unauthorized use, reproduction, disclosure, or sharing of such content with third parties is strictly prohibited.

Access to systems and documentation is restricted based on roles and authorization levels. All users are responsible for acting within their assigned access rights and complying with applicable information security requirements.

Orjin CRS is committed to quality, traceability, and compliance in all services it provides. All processes are documented, monitored, and reviewed as necessary.

The Company fulfills its responsibilities in accordance with applicable laws, regulations, and contractual commitments and reserves the right to update these Terms of Use whenever required.