Probity enhances the capability, performance, and profile of clinical research sites, to provide our Investigators with more study opportunities.
Each site in the PMR network is independently owned and operated. All PMR sites are community-based with investigators that maintain a practice in their specialty.
Study sponsors are given access to our growing consortium of international, high performance sites.
Probity’s support services include:
Access to our clinical trial management
Site training and consultation
Site training and consultation
Budgets and contracts
EXPERIENCE THE EXCEPTIONAL
Over 60 clinical research facilities in USA, Canada, Australia,
Mexico and Chile
Experience in Phase I, II, III, and IV clinical trials
Investigators have conducted more than 1,250 unique clinical trials
Over 31,000 patients followed in those trials
Consistently the top enrolling sites
Responsible for driving the subject recruitment timelines in
many studies resulting in earlier submissions to regulatory
High quality data as evidenced by 56 regulatory inspections (FDA, Health
Canada, & EMEA)
Key opinion leaders (KOL) who have consulted on compound
development for over 270 pharmaceutical companies
Contribute to and guide protocol development for realistic and feasible
Present clinical data due to vast experience with products that are
PMR Investigators have been authors on over 600 research papers, published in medical journals such as:
New England Journal of Medicine
American Journal of Cardiology
American Journal of Hematology
Annals of Internal Medicine
Arthritis & Rheumatism
Australasian Journal of Dermatology
British Journal of Dermatology
British Journal of Urology International
Canadian Journal of Gastroenterology
Clinical Infectious Diseases
Human Molecular Genetics
International Journal of Radiation Oncology Biology Physics
Journal of Cutaneous Medicine and Surgery
Journal of Allergy and Clinical Immunology
Journal of American Medical Association
Journal of the American Academy of Dermatology
Journal of the European Academy of Dermatology and Venereology
Journal of Urology
Medical Journal of Australia
Years of experience
Number of sites
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 for site
Ethics committee submissions
Negotiate budgets and contracts
Liaise with the site
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.
Accurate and timely data
Shortened start-up time
Meeting recruitment targets
Top quality data that meets regulatory standards
Please contact our Feasibility Team at firstname.lastname@example.org. 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.
Pharmaceutical, CRO, or Clinic?
Get in touch with us! Fill out this form to get in contact with a member of the PMR team. We’d love to explore partnering with you!