“As a small start-up medical device company located in the United States we had limited resources with which to conduct our feasibility trial in Australia and New Zealand. That’s where Mobius provided much needed assistance and expertise. Mobius provided us with high quality professional CRO services to initiate, conduct, and close out our trial. Of critical importance to the success of the trial, they identified high quality clinical centres, completed the regulatory submissions to government agencies and ethics committees, developed and supported the clinical trial database and provided much needed expertise regarding local laws and regulations. We would definitely use Mobius for any future clinical trial needs in Australia/New Zealand.“
T.L. Pertile, PhD
Director of Clinical Programs, Osprey Medical
“Mobius Medical has done excellent work initiating, monitoring and assuring prompt data collection from our clinical sites in Australia. Their work is extremely thorough and professional. Their expertise in the regulatory and clinical area is an important asset to a small start-up company like ours. The Mobius Team has allowed us to achieve our study enrollment and data collection milestones on time, in a high quality manner, and within budget. I have recommended Mobius to my CEO colleagues and would work with the Mobius Team again on future clinical trials in Australia and New Zealand.”
Beverly Huss, MS.
President and CEO, Vibrynt, Inc.