Flash Forward is a show about possible (and not so possible) future scenarios. What would the warranty on a sex robot look like? How would diplomacy work if we couldn’t lie? Could there ever be a fecal transplant black market? (Complicated, it wouldn’t, and yes, respectively, in case you’re curious.) Hosted and produced by award winning science journalist Rose Eveleth, each episode combines audio drama and journalism to go deep on potential tomorrows, and uncovers what those futures might re ...
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Content provided by Aleksandra Zuraw, DVM, PhD, Aleksandra Zuraw, and DVM. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Aleksandra Zuraw, DVM, PhD, Aleksandra Zuraw, and DVM or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://staging.podcastplayer.com/legal.
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141: Digital Pathology Tools: FDA Approved
Manage episode 487694347 series 3404634
Content provided by Aleksandra Zuraw, DVM, PhD, Aleksandra Zuraw, and DVM. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Aleksandra Zuraw, DVM, PhD, Aleksandra Zuraw, and DVM or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://staging.podcastplayer.com/legal.
Why do so many digital pathology tools stall before they ever reach patients?
In this USCAP 2025 special sponsored by Muse Microscopy, I talk with Esther Abels, founder of SolarisRTC, regulatory strategist, and the force behind the first FDA-cleared whole slide imaging system.
We break down what startups and established companies must do from day one to succeedbin getting their devices through the FDA. Hint: regulatory strategy isn’t a final step—it’s your starting line.
🧠 What You’ll Learn:
- [00:01:00] Why regulatory planning must start at inception
- [00:03:00] How Esther helped Philips get the first scanner FDA cleared
- [00:05:00] Clinical study design, documentation, and risk strategy
- [00:08:00] Timeline expectations for clearance and review
- [00:10:00] The role of consultants vs. internal regulatory teams
- [00:13:00] Using meta-analysis, synthetic data, and publications
- [00:15:00] How the DPA is driving system decoupling & AI regulatory clarity
🎧 Tune in to learn how to build compliance into innovation—from tissue imaging to AI-powered diagnostics.
#DigitalPathology #RegulatoryStrategy #FDAApproval #ClinicalInnovation #PathologyTools #MUSEmiscroscopy #sponsored #USCAP2025
Support the show
Become a Digital Pathology Trailblazer get the "Digital Pathology 101" FREE E-book and join us!
141 episodes
Share
Manage episode 487694347 series 3404634
Content provided by Aleksandra Zuraw, DVM, PhD, Aleksandra Zuraw, and DVM. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Aleksandra Zuraw, DVM, PhD, Aleksandra Zuraw, and DVM or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://staging.podcastplayer.com/legal.
Why do so many digital pathology tools stall before they ever reach patients?
In this USCAP 2025 special sponsored by Muse Microscopy, I talk with Esther Abels, founder of SolarisRTC, regulatory strategist, and the force behind the first FDA-cleared whole slide imaging system.
We break down what startups and established companies must do from day one to succeedbin getting their devices through the FDA. Hint: regulatory strategy isn’t a final step—it’s your starting line.
🧠 What You’ll Learn:
- [00:01:00] Why regulatory planning must start at inception
- [00:03:00] How Esther helped Philips get the first scanner FDA cleared
- [00:05:00] Clinical study design, documentation, and risk strategy
- [00:08:00] Timeline expectations for clearance and review
- [00:10:00] The role of consultants vs. internal regulatory teams
- [00:13:00] Using meta-analysis, synthetic data, and publications
- [00:15:00] How the DPA is driving system decoupling & AI regulatory clarity
🎧 Tune in to learn how to build compliance into innovation—from tissue imaging to AI-powered diagnostics.
#DigitalPathology #RegulatoryStrategy #FDAApproval #ClinicalInnovation #PathologyTools #MUSEmiscroscopy #sponsored #USCAP2025
Support the show
Become a Digital Pathology Trailblazer get the "Digital Pathology 101" FREE E-book and join us!
141 episodes
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Similar to Digital Pathology Podcast
Flash Forward is a show about possible (and not so possible) future scenarios. What would the warranty on a sex robot look like? How would diplomacy work if we couldn’t lie? Could there ever be a fecal transplant black market? (Complicated, it wouldn’t, and yes, respectively, in case you’re curious.) Hosted and produced by award winning science journalist Rose Eveleth, each episode combines audio drama and journalism to go deep on potential tomorrows, and uncovers what those futures might re ...
…
continue reading
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…
continue reading
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…
continue reading
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continue reading
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…
continue reading
I discuss a variety of topics in both the natural and social sciences, exploring the many fascinating insights that the scientific method yields about the world around us.
…
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We humans could have a bright future ahead of us that lasts billions of years. But we have to survive the next 200 years first. Join Josh Clark of Stuff You Should Know for a 10-episode deep dive that explores the future of humanity and finds dangers we have never encountered before lurking just ahead. And if we humans are alone in the universe, if we don't survive intelligent life dies out with us too.
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…
continue reading
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…
continue reading
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