ARIANNE's services include program planning, regulatory affairs management, clinical services together with site and project management, clinical monitoring, medical monitoring, data management, biometrics, medical writing, and various consulting offerings.
| While working with ARIANNE, you will benefit from the unique, extensive experience and commitment of our staff, the integrity of our systems, and the ability to conduct multi-centers, international successful clinical studies. |
| Each of our offices has its own local proficient regulatory specialist acting as a liaison between ARIANNE and the local regulatory agencies. |
| Each Country Director is highly involved in your study from the beginning until completion to ensure superior service. |
| Our local offices have extensive experience reviewing and preparing documents to the ethics/regulatory committees of their respective country leading to a faster regulatory approval for our sponsors. |
| Country directors, together with their Project Managers and staff, are responsible for thoroughly reviewing all study designs prior to their implementation and ensuring SOP compliance of clinical sites. |
| Each study has a shadow project manager in the US office available to answer US-based Sponsor questions without time delays. Similar settings are available for our international clients. |
| ARIANNE provides global clinical trial support using our own staff. Each of our regional office staff performs all regulatory work, study set-up, and monitoring for ongoing trials -helping sponsors start up faster and reducing pass-through costs throughout the duration of the study. |