WorldCare Clinical conducts all trials with an eye toward successful regulatory submission and approval, and study closeout services are designed to make this process as easy as possible for the sponsor.

Full regulatory consulting and assistance are accompanied by image archival services that allow for central review or simple post-study storage to ensure all data is stored safely and securely for FDA submission – whether directly following your trial, or any time in the future. No matter how we coordinate your trial’s end, you maintain control to the finish.

Regulatory

• Regulatory consulting
• Preparation and submission of documentation for regulatory submissions
• FDA submission assistance, including support at regulatory meetings
• Mock audits of trial data

Image Archival

• Active and post-study storage
• Image library
• Collect, Ready, Hold