Daily Mantra:
I am in control. My discipline shapes my future. I move with purpose, focus, and intention. Temporary pleasures won’t distract me from the greatness I’m building.
You know what’s shocking?
65% of ROP ( retinopathy of prematurity) cases occur in LMICs where pediatric ophthalmologists are scarce.
So meaning lots of children go blind in our settings and they could have been treated.🥲
Truly the work continues @moore_uki 💪
Nothing is more inspiring than hearing stories of people whose sight was saved simply because a doctor caught the signs early.
That exact impact is what drives me and my pal @moore_uki as we build for low resource settings.
Nothing is more inspiring than hearing stories of people whose sight was saved simply because a doctor caught the signs early.
That exact impact is what drives me and my pal @moore_uki as we build for low resource settings.
Nothing is more inspiring than hearing stories of people whose sight was saved simply because a doctor caught the signs early.
That exact impact is what drives me and my pal @moore_uki as we build for low resource settings.
We presented our innovation concept to the Stanford bioengineering team today and i must say engineering is only a small part of great product development and scalable innovation.
We got really great insights from those guys🙌
https://t.co/r4c1dTHNZF
I actually found the link to their recent article on the regulation of medical software.
And the pieces and bits of AI and Machine learning in the medical device.
😂Cut them some slack bro.
@_khalif_07 Do they involve the necessary stakeholders? Do they ensure it serves the medtech community? Do they do a good job at making people know what has been done? Or, do they do so that it’s done?
@moore_uki So i’d say this is a step but it’s not quite it and i also do agree they fall short in having incentives that will see the community grow with the regulations they come up with.
That’s why i said it’s a field we should aim to go to . For the future of the community as a whole.
Might as well now go into the regulatory side of healthcare innovation in the Kenyan Space.
In the US, FDA authorisations of AI-enabled SaMDs have increased significantly in recent years.
Over 1,500 AI-enabled medical devices were FDA authorised as of April 2026.
@moore_uki I believe they dont form regulations haphazardly without having atleast a representative of the necessary stakeholders. They borrow alot from external bodies likes of FDA and EU MDR with the aim to be at par with the Global medtech trends.
@moore_uki They are actually trying to be. Some time back in April they released some guidelines on the regulation of medical software.
And they had some of these considerations listed especially in AI, ML even cybersec.