Frequently Asked Questions

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

• find study opportunities
• 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.

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

Sites will increase their ability to conduct research and receive increased study opportunities.

Please contact our Feasibility Team at feasibility@probitymedical.com. 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.