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27FebFebruary 27, 2019

Overview of Proposed Rule Changes to “Safe Harbor” Regulation

Otis2021-10-15T11:27:55+00:00

Health and Human Services (HHS) is proposing to eliminate safe harbor protection for manufacturer reductions in price on prescription pharmaceutical products to Medicare Part D plans, PBM’s, and Medicaid Managed...

By OtisBlog, Featured0 Comments
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27MayMay 27, 2018

CAR-T Commercial Market Access Brief – A Review of Initial Brand Access at Select US Payers

Otis2021-10-15T11:28:35+00:00

Chimeric Antigen Receptor T-cell (CAR-T) therapies represent a breakthrough in cancer care due to the significant clinical response induced in patients who do not respond to currently available treatments. In...

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15MayMay 15, 2018

A Snapshot of the Conclusions on Long-term Value of Healthcare Treatments Conducted by the Institute for Clinical and Economic Review Group

Otis2021-10-15T11:29:34+00:00

The Institute for Clinical and Economic Review, a non-profit institute evaluates the cost-effectiveness of drugs, medical devices, medical procedures, and diagnostics. The Institute for Clinical and Economic Review has published...

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01NovNovember 1, 2017

US Market Access – Key Considerations in a Changing Environment

Otis2021-10-15T11:30:13+00:00

Many life science manufacturers employ a payer size and control strategy in the US market. While this continues to be viable model, changes in formulary and benefit design result in...

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02OctOctober 2, 2017

Emerging Barriers to Launch Access – the Impact of New Drug Coverage Policies

Otis2021-10-14T05:37:09+00:00

New drug coverage policies provide guidance around a payer’s coverage of new drugs in the time period between FDA approval and P&T committee review. As these policies proliferate, manufacturers may...

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