Government Hospital Manufacturing Medical 
Minnesota Academy of Family Physicians
MARCH 27, 2025
Key proposals included increasing hospital Medicaid reimbursement rates , preventing mid-year changes to prescription drug formularies and establishing a School Health Advisory Committee. The bill passed by a voice vote and was referred to the State and Local Government Committee. Read a summary of S.F.
My Green Doctor
MAY 3, 2025
In This Issue : Why Renewable Energy Belongs in Every Clinic Medical Waste: One Model for Improvement OnTrack with your Sustainability Goals? Latest news & breaking headlines And, in many countries, governments offer financial incentives to install solar panels and even backup batteries. Looking for a tailored approach?
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Georgetown Pediatrics & Family Medicine
MAY 11, 2022
Watering down formula to stretch it out can cause nutritional imbalances in your baby and lead to serious health problems that require hospitalization. Always mix formula as directed by the manufacturer. Infants have been hospitalized from reported use of some homemade formulas. Can I make my own baby formula? Is that safe?
FDA Law
JANUARY 5, 2023
In mid-November, FDA collaborated with the MITRE Corporation to publish an update to the Medical Device Cybersecurity Regional Incident Preparedness and Response Playbook. Combination products are sharing the digital moment with those classified solely as medical devices. FDA has shown a willingness to intervene in this space.
FDA Law
MAY 3, 2021
Recent Department of Justice (“DOJ”) press releases continue to show evidence of reported registrant civil settlements with the Government alleging recordkeeping and reporting deficiencies. The CSA establishes classifications for drugs based on their potential for abuse relative to their legitimate medical use. 21 U.S.C. §
FDA Law
MAY 3, 2021
Recent Department of Justice (“DOJ”) press releases continue to show evidence of reported registrant civil settlements with the Government alleging recordkeeping and reporting deficiencies. The CSA establishes classifications for drugs based on their potential for abuse relative to their legitimate medical use. 21 U.S.C. §
FDA Law
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. The CDS Guidance interprets the Cures Act’s definition of “medical software” that is excluded from the statutory “device” definition, as it relates to CDS software.
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