The Medical Futurist
JUNE 17, 2025
How about having a teledentist consultation? Teledentistry If you are reluctant to go to the dentist, imagine how hard it is for children, patients with special needs or the elderly in nursing homes. This image is then relayed to a machine that manufactures the crown right in the office.
FDA Law Blog
OCTOBER 3, 2022
HHS noticed an increasing trend of illegal kickbacks in connection with speaker programs and in November 2020, the Office of Inspector General issued a Special Fraud Alert on the topic. See 42 U.S.C. 1320a-7b(b). The Alert described several factors that could potentially violate the antikickback statute.
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Imperial Center Family Medicine
JUNE 2, 2025
The liver manufactures new cholesterol molecules and captures excess from circulation for excretion. To eliminate excess cholesterol, specialized liver enzymes transform it into bile salts that get stored in your gallbladder. Contact us today at 919-873-4437 or online to book a consultation.
FDA Law Blog
AUGUST 23, 2021
Kirschenbaum — On August 6, 2021, the Pharmaceutical Research and Manufacturers of America (PhRMA) announced the release of a revised PhRMA Code on Interactions with Health Care Professionals , which takes effect on January 1, 2022. Department of Health and Human Services (OIG) (see our blog post on this Special Fraud Alert here ).
FDA Law Blog
NOVEMBER 20, 2024
Chemical characterization can also be useful in evaluating a change to the materials or manufacturing of a device. FDA suggests that test articles represent the worst-case manufacturing process, and provide the examples that the device undergoes the greatest number of sterilization and/or reprocessing cycles. By Adrienne R.
FDA Law Blog
DECEMBER 7, 2023
There were too many interesting panels and discussions to mention them all, but presentations about DOJ’s and FDA’s coordination deserve some special mention. Gonzalez — The annual Enforcement, Litigation, and Compliance Conference put on by the Food and Drug Law Institute (“FDLI”) took place in Washington this week.
FDA Law Blog
MAY 20, 2021
Investigators likely consult with DEA headquarters about the registrant’s compliance with required reporting and review its registration category, status, and authorized controlled substances to assess whether it may be conducting unauthorized activities. Accountability Audit.
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