This course is accepted by the California Department of Public Health – Food and Drug Branch.
This is a web class. After completing registration, check your email for the URL for the class and the enrollment key. If you do not see the email after 10 minutes, check your SPAM or JUNK mail folder.
Students review pre-recorded presentations covering the required content for certification.
Following each presentation the student takes the final exam. Students may review the content of any section as many times as they want. Students may take the exam for each section as many times as needed to get a passing score (85%). Students get instant feedback on test performance.
When you pass all the topic exams, click on the appropriate link at the bottom of the page, to request the documentation appropriate for the agency the student is applying to.
Training Certificates for Exemptees are sent to the address provided at the end of the course via FedEx Express Service every Monday morning, unless a different schedule is indicated in the web room entry page. Oftentimes we send out certificates on a daily basis.
The class is $525 per student when registered through Cvent, a secure online booking service. There are no additional fees unless you choose to add FedEx Overnight Delivery, or lose or misplace your certificates and need reprints.
The applicant must demonstrate knowledge and understanding of:
Dangerous drugs and devices
Distribution of controlled substances
USP Storage conditions
The safe storage and handling of home medical devices
“The increased demand for CPAPs and disposables creates opportunities for home medical equipment (HME) and durable medical equipment (DME) suppliers. But a word of caution: The supplier can have no involvement with a home sleep test (HST) administered to a patient covered by Medicare fee-for-service (FFS).”
“In short, Medicare will not pay ABC for the CPAP if ABC is the provider of the sleep test. That term is defined as “the individual or entity that directly or indirectly administers and/or interprets the sleep test and/or furnishes the sleep test device used to administer the sleep test.””
““Health care trends suggest that 2.5 million number is just going to continue to grow as more people opt to age in place,” Marriele Mango, lead author of the study and resilient power fellowship program associate for Clean Energy Group, told HHCN. “In the end, energy security just isn’t there for them in the way that it is in a nursing home, assisted living home or a hospital.”
In the event of a natural disaster, lack of energy security can be fatal.”
The FBI & DOJ targeted alleged schemes involving the payment of illegal kickbacks and bribes by DME companies in exchange for the referral of Medicare beneficiaries by medical professionals working with fraudulent telemedicine companies for back, shoulder, wrist and knee braces that were medically unnecessary. Some of the defendants allegedly controlled an international telemarketing network that lured over hundreds of thousands of elderly and/or disabled patients into a criminal scheme that crossed borders, involving call centers in the Philippines and throughout Latin America.
Budget neutrality dampens certain oxygen reimbursement | HME News
“These additional cuts for home oxygen therapy are certain to impact providers and patients in rural and other non-CBA areas,” stated AAHomecare in a bulletin. “Since CMS has repeatedly made it clear that they do not believe they have the statutory authority to address the budget neutrality offset, the HME community needs to make this a priority for advocacy efforts in the 116th Congress.”
“The purpose of the retail awards competition is to promote and recognize products that contribute to providers’ bottom lines though cash sales. Representatives from seven companies made their case to session attendees, who along with judges, voted on their top three choices.”
The Sherman Food, Drug, and Cosmetic Law, among other things, prohibits a person from conducting a home medical device retail facility business in the state without a valid license from the State Department of Public Health. Existing law requires the department to inspect each place of business prior to issuing a license, and further requires the department to inspect each licensee at least annually.
This bill would modify, until January 1, 2023, the requirement for the department to inspect a licensed home medical device retail facility business if it is accredited, as specified, by an accreditation organization approved by the federal Centers for Medicare and Medicaid Services. If so accredited, the bill would authorize the department to conduct an inspection only upon a complaint made to the department regarding the licensee. For a licensee that is not so accredited, the bill would continue to require the department to conduct an inspection at least annually.
“Another data point shows just how greatly Medicare’s importance as a revenue driver for HME has dropped. In addition to Medicare’s 16 percent share, Medicaid accounted for 15 percent of HME spending, and all other sources, such as private payer and retail sales, represented 68 percent of HME spending.”