Adam Raymakers

@araymakers.bsky.social

Health economist & research fellow with the Program on Regulation, Therapeutics, & Law (PORTAL) at Harvard Medical School. Interests: drug pricing/policy, health technology assessment, climate change. www.linkedin.com/in/araymakers

Excited to share this new work co-authored with Leah Rand & Mike Paulden in Health Affairs Forefront! There's been lots of talk about the relationship between innovation, cost-effectiveness analysis, and incremental cost-effectiveness thresholds. (1/4) www.healthaffairs.org/content/fore...

Cost-Effectiveness Thresholds: Overvaluing Innovation, Undervaluing Health | Health Affairs Forefront

To address the gap between opportunity costs and cost-effectiveness thresholds, we must identify the marginal cost of a unit of health for health care systems.

healthaffairs.org

Interested in how climate impact could be incorporated into health technology assessment? We leverage real-world evidence for triple therapy inhalers, estimates of the carbon footprint on inhalers, and bring it together in an HTA framework! #ISPORAnnual

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It's been a few years but really excited to be back at Canada's Drug Agency Symposium 2026! Off to a great start with a plenary on international approaches to HTA with Suzanne McGurn, Sarah Emond, Natalie M., and Yannis Natsis. #CDAAMC26

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Two abstracts accepted for ISPOR 2026 in Philadelphia! The 1st abstract illustrates a way to include climate impact into health technology assessment. The 2nd is an analysis of spending on new gene therapies for recessive dystrophic epidermolysis bullosa. See you in Philly!

The FDA is increasingly turning to ad hoc expert panels instead of federal advisory committees for external advice. FDA watchers generally agree these expert panels "are likely unlawful," USC Schaeffer's @profgenkanter.bsky.social tells Regulatory Focus.

Experts argue recent FDA expert panels may violate FACA requirements

The US Food and Drug Administration@s (FDA) increasing reliance on holding expert panels, rather than advisory committees, for external expert advice may violate the Federal Advisory Committee Act (FA...

raps.org

We would like to recruit a stellar junior faculty member in the Division of Child Health Research and Policy @deptpopmed.bsky.social at Harvard. Please circulate this announcement widely! www.populationmedicine.org/divisions-ce...

Faculty Positions | HPHCI: Department of Population Medicine

populationmedicine.org

Harvard Pilgrim Health Care Institute@deptpopmed.bsky.social · 6mo ago

📢 We’re Hiring! @cherpdpm.bsky.social is recruiting for a full‑time position with a proposed academic appointment as Instructor or Assistant Professor of Population Medicine at Harvard Medical School. Full job details: tinyurl.com/233s3vjm Questions? Contact cherp@hphci.harvard.edu. Apply today!

We’re hiring! Join our team as a: Junior Faculty (Instructor or Assistant Professor).

'The FDA will ask Sarepta to stop shipping its Duchenne muscular dystrophy treatment Elevidys, an HHS official said, in what could be a final blow to the company’s hopes for the product following two patients’ deaths.' via @endpts.com endpoints.news/fda-asks-sar...

Breaking: FDA will ask Sarepta to stop selling Duchenne treatment, following patient deaths

FDA to request Sarepta halt shipments of DMD drug Elevidys after two patient deaths, HHS official says. Trading of $SRPT shares paused after decline.

endpoints.news

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The clinical aspect & decision aside, it's problematic for health systems that BioMarin priced Brineura at $1 million. If companies didn't charge these prices, decisions would be easier & less restrictive. Note: Brineura's net sales in 2024 were $170 million (US alone). www.cbc.ca/news/canada/...

Vancouver Island family heartbroken as B.C. stops funding $1M drug for girl with terminal condition | CBC News

Charleigh Pollock's mother says the family has gone through a roller-coaster of emotions since learning the B.C. government has pulled funding for the drug their daughter needs for the rare and termin...

cbc.ca