California Academy of Family Physicians (CAFP)
MAY 14, 2025
Key Health Care Budget Proposals: Proposed Medi-Cal Cuts and Enrollment Changes Medi-Cal, California’s Medicaid program, is typically funded through a partnership between the state and the federal government. The asset limit for a household would be $2,000 for an individual and $3,000 per couple.
FDA Law Blog
NOVEMBER 27, 2023
According to the government, these companies knew as early as 2012 that their dehumidifiers were defective, in that they could overheat and catch fire. At the time, in 2016, the Gree Companies’ settlement for $15.45 The government charged these individuals with conspiracy (18 U.S.C. § See 15 U.S.C. § 2070.
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Family Physicians of St. Joseph
SEPTEMBER 25, 2018
However, in 2016 they began to realize that the rules and oversight from insurance companies and government entities were creating an environment that took the focus of physicians away from the patients and onto their computers and the completion of irrelevant busywork.
FDA Law Blog
OCTOBER 13, 2024
Designed to incentivize the development of drugs for pediatric rare diseases where such development may not otherwise have occurred, vouchers may be granted for drugs for serious or life-threatening rare diseases where the serious or life-threatening manifestations primarily affect individuals aged from birth to 18 years.
FDA Law Blog
AUGUST 8, 2024
Governors, state cannabis regulators, law enforcement groups and local governments weighed in, as did marijuana advocates and opponents, marijuana industry associations, Members of Congress, federal law enforcement groups, healthcare and human rights groups, unions and trade associations, and private individuals. 53,688 (Aug.
FDA Law Blog
SEPTEMBER 6, 2022
This Draft Guidance, when finalized, will replace the Final Guidance issued just six years ago (the 2016 Guidance). Changes from the 2016 Guidance. Livornese — FDA recently published a Draft Guidance entitled “Charging for Investigational Drugs under an Investigational New Drug Application: Questions and Answers” (the Draft Guidance).
FDA Law Blog
OCTOBER 10, 2022
The CDS Guidance interprets the “medical software” carve-out of the 21st Century Cures Act (2016) as it pertains to Clinical Decision Support (CDS) software functions. Specifically, the guidance interprets the Cures Act’s four criteria for exclusion of CDS software functions from FDA’s medical device jurisdiction (so-called “Non-Device CDS”).
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