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I shared this with my husband, he is a microbiologist and a professor. He could use something like this as a learning tool for undergraduates, PLUS he can use it as a way for them to keep up to date (contributing to the community, subscribing to new research) as well. Great idea!
@brynatweets That's awesome. We'd love to connect with him actually and get his feedback. He can email us directly: team@hdphealth.com Maybe we can hire some of his students. :) :)
Really excited about this. I love how this not only demystifies medical research for the layhuman, but also exposes med school PhDs and researchers to the latest and greatest in relevant science.
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Finally a product that solves real problems. Great job Kumar and Brian! I look forward to learning more about Lupus through your product.
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This is excellent. It's such a shame that most papers are inaccessible or completely missed due to lack of time. Thanks for sharing!
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Great idea. Are there plans for support in other languages than English?
@kexino Could you clarify your question?
Do you mean the output summary or the article you put in? (I'd actually be curious to see research papers in languages other than English.)
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@datarade Yes, to have the output summary in other languages.
@kexino if you plan on those languages, simply email me kumar@hdphealth.com and let us know. We'll do what we can to push it out in German or French as per your request.
@fotoflo It's free.
If we observe a pattern of a student posting the requests, we'll inquire to make sure it's not for homework.
Our number one priority is sick patients, their families, and people trying to make sense of complex diseases in general.
@fotoflo That being said, our turn around time will vary. As well, there's some research that's not easily translational. For example, explaining a monoclonal antibody has a ton of dependencies in biology to explain to someone.
@fotoflo We help patients aggregate their full medical records and map them against a huge list of clinical trials criterion.
10 years ago, when I aggregated my own records, it cost me several thousand dollars. As well, there was no viable way to search for clinical trials. It was tough. As well, most patients don't know generic drug names and/or regimens their on.
Fast forward to today, there's technologies that allow us to aggregate our medical records (partly motivated by the notion of Population Health and the new Healthcare system) and as well a robust clinicaltrials.gov site that makes it easy to search.
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