Probity Medical Research Inc. provides support services to independent, clinical research sites, and works with sponsors to identify suitable sites.

• Find study opportunities for site
• Complete feasibility
• Ethics committee submissions
• Negotiate budgets and contracts
• Liaise with the site
• GCP training
• Provide solutions to study issues
• Create advertising and recruitment plans
• Provide and manage regulatory documents
• Provide monthly study payments
• Provide access to our online clinical trial management platform
• Preparation for regulatory inspections

Sponsors will receive access to experienced, high-performance sites, that are supported by PMR throughout all stages of a study.
Sites will increase their ability to conduct research and receive increased study opportunities.

Benefits include:

• Accurate and timely data
• Shortened start-up time
• Meeting recruitment targets
• Top quality data that meets regulatory standards

Please contact our Feasibility Team at [email protected]. Should you require consulting services on protocol design and conduct, our Feasibility Team will reach out to our investigators to provide you with independent consulting services.