FOCUS ON MEDICAL DEVICES
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Navigating Complex Trials to Approvals
Biorasi’s methodology leverages our TALOS Ecosystem, an integrated technology and program management platform designed exclusively for Clinical Research. The efficiency of the TALOS Ecosystem offers greater success for our sponsors and allows faster trial completion while minimizing risk of failure.
Medical devices are a unique field with a unique approach to regulatory approvals and clinical trials. Biorasi combines deep expertise in the specialized area of medical devices, and combines it with decades of therapeutic area excellence and our industry leading processes to make your device journey from idea to market as easy as possible
Authors: Geetesh Shrivastava, Associate Director of Clinical Monitoring; Jennifer Dennis-Wall, PhD, Lead Scientific Writer Back in August, we published a blog addressing themes that are
When recruiting patients with hard-to-enroll indications, such as rare diseases, it is sometimes necessary to dip into creative resources for finding sites. Sometimes this means
The liver does many important things in the body, such as filtering of the blood and metabolizing all compounds, including food and drugs, that enter
A True Medical Device Expert
What are the common issues medical devices face when seeking regulatory approval? Does my device even need regulatory approval? Can it be approved in multiple venues simultaneously? What if my device is a drug/device hybrid?
At Biorasi, we hear questions like these all the time from medical device companies seeking to get their product to market in the United States and abroad. We’ve spent a lot of time, and enlisted a lot of the top experts in the field, to come up with the best answers for our clients and make the device approval proccess as simple and painless as possible. As a true medical device CRO, we offer more than just plans and proposals: we offer answers, and the peace of mind that comes with knowing your device trial is in good hands.
Some of our medical device approval services include:
- Medical device program development consulting
- Regulatory consulting for medical devices
- Multi-venue medical device approval plans
- Medical device clinical trial management
- Drug/Device hybrid clinical trials