Home / Newsletters / Regulatory and Reimbursement Newsletter | November 2025
Regulatory and Reimbursement Newsletter | November 2025
The Latest in Regulatory and Reimbursement
Biocom California submitted its comment letter responding to the Department of Commerce’s Section 232 investigations on the national security effects of imports of personal protective equipment and medical devices. The FDA announced the first nine recipients of the Commissioner’s National Priority Voucher, publicly released internal filing checklists, and published a new draft guidance reforming biosimilar regulatory recommendations. CMS temporarily recalled furloughed staff to support open enrollment for Medicare and Affordable Care Act plans and published its final guidance for the Medicare Drug Price Negotiation Program for Initial Price Applicability Year 2028.
Biocom Comments on Recent Section 232 Investigation
Biocom submitted a comment letter responding to the Section 232 investigations on the national security effects of imports of personal protective equipment and medical devices.
The FDA is reforming aspects of its regulatory approach for biosimilars. The agency released a new draft guidance which would reduce the need for comparative studies and it plans to finalize a separate guidance regarding interchangeability and switching studies.
FDA Releases Filing Checklists
The FDA publicly released application filing checklists used internally by CDER staff to determine if a submitted application is complete and reviewable. This is part of an agency effort to increase transparency into FDA filing procedures.
Furloughed CMS Staff Return to Support Open Enrollment
Despite the ongoing government shutdown, furloughed CMS staff will temporarily return to the agency to support open enrollment for Medicare and Affordable Care Act plans.
Request for Comments
Biocom California welcomes feedback from members on the following draft guidance document. Click here to submit comments via email.
The guidance provides information about the use of the accelerated approval pathway for RMAT-designated therapies.
The guidance describes considerations in the clinical development of regenerative medicine therapies and opportunities for sponsors to interact with CBER review staff.
This guidance may be of interest to developers of biological products.
Congratulations to Biocom California member, Bayer, on the FDA approval of its drug, Lynkuet, for the treatment of moderate to severe hot flashes due to menopause.
Biocom California
For over 30 years, Biocom California has helped move the life science industry forward with transformative resources that enable companies to make meaningful connections. We connect our members to each other so they can collaborate and work stronger and smarter together. We connect organizations to capital investment and purchasing solutions so they can grow faster and work more efficiently. We’re their link to advocacy that fights for innovation and we provide an environment where their business and talent can thrive. Biocom California is how the life science industry gets connected.