Tips for Getting Your Device into a Hospital

Trying to get your new medical device picked up by a major hospital? Here are some insider tips for getting a foot in the (operating room) door.

Marie Thibault

October 8, 2015

4 Min Read
Tips for Getting Your Device into a Hospital

Trying to get your new medical device picked up by a major hospital? Here are some insider tips for getting a foot in the (operating room) door.

Marie Thibault

Your medical device has made it through all the early hurdles: design, user experience, clinical trials, and FDA. Next comes commercialization, but becoming a regular hospital purchase is harder today than ever. Hospitals want to ensure that they are getting value and improved patient outcomes for each new device they introduce.

Hospitals often have committees to evaluate new technology acquisitions, so new devices need to pass this committee's muster before making it into the hands of physicians and surgeons.

At this week's MD&M Philadelphia conference, Neil Sheth, MD, assistant professor of orthopaedic surgery at the Hospital of the University of Pennsylvania, was asked to give some advice on how new devices can optimize their chances with hospitals. Sheth, who sits on his hospital's new technology committee, told the audience that device makers always need to be thinking about what problem their device solves, how it improves patient metrics, and lowers costs.

Besides that, Sheth gave listeners the following practical tips:

  • Have a champion for the device: "You kind of need to have a physician champion for that device and they've got to really have a voice . . . to say, 'Hey, I'd like to use this device,'" Sheth says. He adds that any caregiver in the hospital (it doesn't need to be a surgeon from the operating room) can present to the committee, though it is probably an advantage to have a committee member advocating for your technology, since they are most familiar with how the committee might respond to specific issues. All the better if your champion is a prominent leader in their treatment field.

  • Have an easy-to-deliver message: The hospital staffer who is advocating for the new technology will present a few slides on the device, focusing on how it tackles an unsolved problem and/or reduces costs. "They have maybe three to five slides—background information on the medical device, they demonstrate what the problem is, how this device can actually solve that problem or make that problem much easier to address for the patient, what the cost is . . ." Sheth says. That means device makers need to emphasize these points repeatedly when introducing the device to potential champions, and make those advantages easy to see immediately to ensure the user's experience is pleasant and memorable.

  • Try to get several users and devices included in any trial period: If your device impresses the committee, it may get a trial run. Sheth explains, "After the presentation, the committee meets and will say, 'This makes a lot of sense. It sounds like this is a really common problem we're seeing and . . . it was addressed well.' They'll allow them some short-term—whether it's a month, six weeks, three months—of a trial period, where they'll actually start collecting data almost like a pilot study. Say, 'Is this doing better for us?'" Trying to advocate for a larger trial to get more useful data might be helpful, though Sheth says the committee usually chooses the size, deciding how many trial users there will be and how many devices will be used.

  • Be persistent and patient: Sheth revealed that earlier in his career, he presented to a technology acquisition committee. He was passionate about a specific device that he believed would help reduce blood loss during revision surgeries. Despite what he believed was a relatively inexpensive device cost for a lengthy surgical procedure, it still took him months of presenting and re-presenting data to convince the committee to allow a trial. The process of starting to advocate for the new technology to being able to use it regularly in his revision surgeries took 2.5 years, he says. Costs play a big part in addition to the clinical benefits. "It's a challenging process," Sheth admits.

Want to catch up on the latest in medical device innovation? Register for the MD&M Minneapolis conference, November 4–5, 2015.

Marie Thibault is the associate editor at MD+DI. Reach her at [email protected] and on Twitter @medtechmarie

[Image courtesy of ARTUR84/FREEDIGITALPHOTOS.NET]

About the Author(s)

Marie Thibault

Marie Thibault is the managing editor for Medical Device and Diagnostic Industry and Qmed. Reach her at [email protected] and on Twitter @MedTechMarie.

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