
Exploring the people, challenges, and opportunities impacting the global #medtech regulatory, reimbursement and policy communities. Likes,RTs,etc ≠ endorsement.
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Joined April 2019
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Market Pathways | MedTech Regulatory & Policy retweeted
The 2025 #NIH Public Access Policy may still leave NIH-funded investigators facing new article processing charges for immediate public access, with an estimated upper-bound annual cost of more than $100 million. ja.ma/4hpzzSm
Market Pathways | MedTech Regulatory & Policy retweeted
.@MedTechStrat, @Market_Pathways, and the #medtech community are already making plans for Boston.
Come meet some members of our team at Booth #1136 at #MedTechCon:
Market Pathways | MedTech Regulatory & Policy retweeted
The European Medicines Agency's Committee for Medicinal Products for Human Use is planning to update a 2018 guideline on good pharmacogenomic practices.
hubs.la/Q04zBkY50
Market Pathways | MedTech Regulatory & Policy retweeted
Finalizing guidance on artificial intelligence-enabled devices throughout their product lifecycle and on pre-determined change control plans tops the to-do list for the FDA Center for Devices and Radiological Health for fiscal year 2027..
hubs.la/Q04zg7Dk0
Market Pathways | MedTech Regulatory & Policy retweeted
Michael Davis, the director of the FDA's Center for Drug Evaluation and Research, stated that increasing the availability of generic versions of glucagon-like peptide-1 (GLP-1) medications is a top priority for the agency to lower costs for Americans.
hubs.la/Q04yzsDS0
Market Pathways | MedTech Regulatory & Policy retweeted
Some people leave a mark on an industry that lasts far beyond their lifetime. We mourn the loss of our colleague, friend, and co-founder @DCassak. His kindness and legacy will not be forgotten: bit.ly/3TROZpv
Market Pathways | MedTech Regulatory & Policy retweeted
.@MedTechStrat, @Market_Pathways, and the #medtech community are already making plans for Boston.
Come meet some members of our team at Booth #1136 at #MedTechCon:
Market Pathways | MedTech Regulatory & Policy retweeted
CDRH Director Michelle Tarver, MD, PhD, joins
@Filmoreorless of @Market_Pathways at #InnovationSummit this year for an opening keynote & fireside chat on TAP, early feasibility studies, FDA-CMS alignment, #AI, cybersecurity & more. Bring your questions: bit.ly/4h7JsTs
Market Pathways | MedTech Regulatory & Policy retweeted
It is with profound sadness that we share the news that David Cassak, co-founder and co-editor of @MedTechStrat, passed away peacefully this weekend.
(🧵)
Market Pathways | MedTech Regulatory & Policy retweeted
Stay closer to what’s shaping the #medtech industry. 📖
Claim a free print issue of @MedTechStrat or @Market_Pathways and get expert insight and analysis delivered straight to you.
Claim your free issue: bit.ly/4xw0rpv
The FDA is seeking public input on considerations for the regulation of generative AI-enabled medical devices. We’ve put out a discussion paper, and we’re inviting feedback by October 19, 2026.
fda.gov/news-events/press-an…
Market Pathways | MedTech Regulatory & Policy retweeted
One of this month's Docs of the Month, this Council of the EU progress report breaks down the latest developments in EU MDR and IVDR reform and where negotiations are headed. Read the rest of the Doc here: bit.ly/4wBT7YG #MedTech
Market Pathways | MedTech Regulatory & Policy retweeted
Halfway through 2026, 1 resource stands above the rest. Pathways' Document Depot is our most viewed resource of the year, helping #medtech professionals stay on top of global #regulatory updates: bit.ly/3TFQ17x
Market Pathways | MedTech Regulatory & Policy retweeted
890+ pages that could impact #medtech. @CMSGov finalized NTAP changes with a 2-year transition for Breakthrough Devices. Download the nearly 900-page FY2027 IPPS rule PDF: bit.ly/4zj1eeP
Market Pathways | MedTech Regulatory & Policy retweeted
2029 may seem far off, but the MDR/IVDR transition continues to reshape the #medtech landscape. See how manufacturers and #notifiedbodies are tracking progress across Europe. Does this reflect what you're seeing?
Market Pathways | MedTech Regulatory & Policy retweeted
The smartest people in #medtech stay ahead of change. Market Pathways delivers expert insights on policy, regulation, #reimbursement, and market access so you can make better decisions. Subscribe today: bit.ly/4biPNt5
The FDA is taking another step to phase out petroleum-based food dyes in support of the #MAHA agenda.
The agency issued a final order revoking the authorized use of Orange B and is proposing to revoke the authorized use of Citrus Red No. 2 after determining they are no longer used by industry.
Market Pathways | MedTech Regulatory & Policy retweeted
The smartest #medtech conversations happen here. Explore the @Market_Pathways podcast for expert insights on policy, strategy, and #reimbursement. Listen: bit.ly/4wy078v
Market Pathways | MedTech Regulatory & Policy retweeted
The next chapter of #MedTech regulation is already taking shape. Hear @Filmoreorless's take on MDUFA VI and the changes worth watching. July 24 at 11 AM ET. Mark your attendance here: bit.ly/4gBdQqH
Market Pathways | MedTech Regulatory & Policy retweeted
Struggling with #MDR/IVDR classification? The updated EU Borderline & Classification Manual (v5, April 2026) offers key guidance. Explore it and access more in Pathways’ Document Depot: bit.ly/4dZDRyB


























