“Operational Excellence, Seamlessly Delivered”

At Clinitude, we provide flexible, hands-on operational support across the entire clinical trial lifecycle. Whether you need full-service execution or targeted functional support, our experienced professionals integrate seamlessly with your team to keep your trial on track, on time, and on budget. From study start-up to end of trial, we help streamline operations while upholding the highest standards of compliance and quality.

• Regulatory submissions to health authorities and EC/IRBs
• Study start-up coordination, incl. site feasibility and selection
• (e-)Trial Master File (TMF) set-up and management
• Service provider and site selection, management and oversight
• Clinical & Regulatory Project Management
• Clinical data management: study set-up, conduct, and close-out
• Site Management
• Administrative and project support
• Specialized Delivery Expert (formerly known as FSP)
• On-demand operational resources tailored to your needs