With extensive experience in both, the conduct of studies at the investigational site as well as the management of studies from the sponsor’s perspective, Wahoo Clinical understands the requirements and challenges of both sides.

Wahoo Clinical is accustomed to conduct studies for European, US, Japanese and Chinese sponsors with data being submitted to the relevant regulatory authorities.

Clear and transparent communication with all parties involved, pro-active following-up and reporting of all issues affecting the client and the project is applied to all services to ensure smooth and successful completion of the clinical trial.

Services include:

• Clinical study management all phases
• Clinical protocol and report development
• Clinical trial design
• Communication with regulators
• Directing cross-functional teams and third party vendors
• Study start-up activities
• Recruitment strategies including ethnic sub-populations
• Study site management
• Monitoring of protocol compliance and data integrity
• Assurance of GCP and safety reporting requirements
• Training of site staff