Tim Davis (@digital_timd) profile picture

Pharma & Digital Health Guy. Currently enjoying life as VP @veevasystems Also interested in @LUFC and cycling.

London
Joined June 2013
Photo by Tim Davis (@digital_timd)Photo by Tim Davis (@digital_timd)Photo by Tim Davis (@digital_timd)Photo by Tim Davis (@digital_timd)Photo by Tim Davis (@digital_timd)Photo by Tim Davis (@digital_timd)Photo by Tim Davis (@digital_timd)
Its Friday. Let's make someone's day with some spares we have! Retweet and we will choose someone for a free Berardi mug #lufc
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McKinsey: Up to $250B of US health spending could become virtual scoop.it/topic/public-health…
How is COVID-19 affecting real-world patient experience research? Our CEO @digital_timd shares his thoughts in this podcast: bit.ly/3bVitXO
Here are 2 updated charts showing the countries with the most #covid19 cases overall & per capita in countries with at least 4m residents and 5k cases. statista.com/chart/21176/cov…
The #FutureFund opens for applications on Wednesday 20 May. Find out more: bit.ly/2LCfVmp
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Today I will be relentlessly commenting on the news in real time from a position of ignorance. I hope you will join me.
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We're excited to have launched our new community for those living with (and those with experience of) urea cycle disorders. Watch this space for articles and news on #UCD! #UreaCycleDisorder #OTCD raremark.com/urea-cycle-diso…
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"If no one's going to help me then I'm just going to have to help myself" - a sentiment we're all familiar with! Thank you Shamonica for sharing your story. We recorded this video in partnership with @SCDAAorg #sicklecell
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Families will be the activators of change in rare disease research Flexed biceps. Our founder @JulieAnnWalters speaks about the power of patient groups in this podcast by @Genialis: bit.ly/2xv5uNU
Raremark helps researchers develop treatments for rare diseases by collecting real world experience data that's unavailable elsewhere. Have a look at some of the data we've gathered: bit.ly/3aYfWfi
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we are all edward hopper paintings now
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🔊 How can AI and technology empower patients to manage their own health, find treatments and feel connected? Our Head of Research & Analysis @PeteChan100 shared his thoughts at the @camraredisease RARE Summit #RAREsummit19 bit.ly/2Ie6TKu
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It can sometimes be difficult to articulate what living with a chronic illness is like. Using the spoon theory could help: bit.ly/32J4YY0
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How do we keep patients at the center of clinical trial research? Our CEO @digital_timd speaks to @Pharmavoice: bit.ly/32MrsYf
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Rare Disease Day might be over but our job isn't. @PeteChan100, our Head of Research & Analysis, takes a deeper look at the benefits of investing in patient trust in the long term: bit.ly/384m6s9
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Immensely proud to see our co-founder Julie Walters named as a global shaker for rare diseases bit.ly/3cnAXS4
Our list of Rare Disease Champions is packed full of Patient Power 🦓💪 On #RareDiseaseDay learn more about these incredible people and their fight to raise awareness of some of the world's most underserved diseases. globalshakers.com/shaker-lis… #rarereality #ShowYourStripes #LeapDay
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Making history: First AI-developed drug to be tested in human trials  #esante #hcsmeufr #digitalhealth via @dgodefroyfr scoop.it/topic/e-health-star…
There have been over 50 film submissions for Rare Film Festival 2020. You can watch the films and vote for your favourite today! Voting is only be open until tomorrow so you need to be quick! #rarefilmfestival @rarediseaseuk bit.ly/39g0fzD
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We're sharing community stories in the lead up to #RareDiseaseDay. Holly has myasthenia gravis: “It’s a balancing act, constantly knowing where you are at and what you are capable of, and saying ‘I need help with this’ or ‘I can’t do this right now’ and knowing that that is OK.”
We're sharing community stories in the lead up to #RareDiseaseDay, like this powerful quote from a dad whose child has a rare disease. “The child you have after you learn their diagnosis is the same child you had before...” raremark.com/articles/stay-s…
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