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Mediprobe Research focuses on Phase II-IV clinical trials with topical and oral formulations. In conjunction with our sponsors we have proven expertise in developing protocols designed to address specific research questions. With over 20 years of combined experience in clinical trials, access to a central IRB (REB) and a potential patient pool of 750,000 patients we are able to conduct superior quality research that exceeds our client's expectations.
We customize study designs based on the objectives and requirements of our pharmaceutical clientele.
Mediprobe has a team of clinical research coordinators with experience in the conduct of clinical trials.
All subjects are examined by a physician. We have a photographic studio with Canfield state-of-the-art camera systems for dermatological studies. Our expertise and the presence of a large patient database enables us to start clinical trials efficiently and recruit subjects quickly. We advertise for subjects regularly on the television, newspaper, radio, in flyers, and we conduct patient education seminars. In addition, The University of Western Ontario with a population of 29,000 students is located only minutes away from the clinic.
We comply with ICH-GCP guidelines and ensure that the clinical trials are conducted according to the study protocol, the sponsor guidelines, and regulatory requirements.
Our Advantages
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World class centre for Phase II-IV clinical trials in dermatology
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On site phlebotomy with expertise in processing and shipping plasma samples to bioanalytical laboratories |
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Central location in London with easy access from Highways 401 and 402, and London Airport |
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Minutes away from University of Western Ontario with approximately 29,000 students |
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In-house protocol and case report form development |
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Expertise in regulatory submission to Health Canada, independent Research Ethics Board, and FDA |
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