Leverage our expertise in medical devices to streamline trial logistics and ensure seamless integration with our comprehensive clinical trial services, maximizing efficiency and data quality throughout your study.
Medical Device Trials
Precision evidence to support product approvals
Generate reliable evidence for medical device trials
The pathway to approval for new diagnostic and therapeutic products, or combination drug/device products, isn’t always straightforward. Signant blends proven evidence generation and trial optimization solutions with clinical and operational expertise to help you meet your protocol and product goals.
With an understanding of the nuances inherent in medical device research and our comprehensive solutions, Signant is ideally placed to support your study objectives. From early feasibility to post-marketing, our technology solutions and in-house scientific expertise help you capture reliable evidence to support regulatory decision-making, and streamline and optimize trial operations.
Achieve your product goals
Signant can facilitate your efforts to develop new medical device technologies as well as identify novel applications for existing products.
Electronic data capture
Leverage our easy to use, comprehensive and agile EDC solution to capture and manage all your clinical data. Set up in 4-6 weeks, sites love the intuitive interface and guided workflows which makes it easy to get their jobs done.
COA data capture
Collect patient- and clinician-reported outcome data electronically from patients at home or at site with our flexible eCOA platform, which includes a library of common measures.
Inventory management
Ensure the right devices are available at site for the right patients at the right time with our rapid-deploy RTSM system, supported by global logistics teams familiar with country-specific importation regulations.
Multinational studies
Run your studies across multiple countries with ease by leveraging Signant's global scale and operational operational capacity. With project teams in your time-zone, we're easy to work with.
Endpoint selection & protocol design
Our clinical science and medicine team, experienced in all therapeutic areas, can advise and provide guidance on all aspects of trial design including patient-reported outcome measure selection, and trial optimization using technology.
Telemedicine
Perform follow-up and between-visit consultations via video using our secure, compliant telemedicine platform.
Patient engagement
Provide study information, up-to-date study visit schedules, patient reminders and alerts to guide patients through each step of the trial, using the same app used to collect PRO data.