The Digital Health Corner

JUNE 14, 2017

According to most recent statistics from the Office of the National Coordinator, use of EHRs has increased from 20% in 2004 to 87% in 2015. There are hospitals within the same healthcare system in many places with disparate EHRs which do not talk to each other or exchange information. in the approval process of drugs.

Patient Satisfaction 87

Patient Satisfaction Hospitals FDA Governance 87

SQA

OCTOBER 18, 2023

The US FDA has already recognized the ability of 16 EU Member States to conduct GMP inspections of manufacturers of veterinary medicinal products. At the same time, the EU has recognized the US FDA as an equivalent authority to carry out these inspections. times the intended dose and required intervention in a hospital.

FDA 40

FDA Compliance Licensing World Health 40

Hall Render

FEBRUARY 2, 2024

Vincent North in Sherwood Washington Regional Medical System Names Lucas Campbell as VP & Chief Transformation Officer 4 more Arkansas hospitals awarded federal funds Arkansas Legislative Council approves Department of Human Services’ requests for $13.4M

Nursing Homes 40

Nursing Homes US Department of Health and Human Services Nurses Hospitals 40

Bill of Health

AUGUST 29, 2022

1] E.g., Anna Edney, Kids’ Covid Hospitalizations Hit Record in U.S. 31, 2021), [link] (describing a record number of pediatric COVID-19 hospitalizations due to the omicron variant). [2] A full form of this Article is forthcoming in the Minnesota Journal of Law & Inequality Vol. Omicron Surge , Bloomberg (Dec. 3d 868, 874 (Wyo.

COVID-19 Vaccine 130

COVID-19 Vaccine COVID-19 Informed Consent Governance 130

Drug & Device Law

DECEMBER 4, 2023

CPAP II shrugs off plaintiffs’ repeated allegations that defendants “failed to apprise the FDA” of this or that, with the excuse that plaintiffs don’t really “rely” on them. Northwestern Memorial Hospital , 134 N.E.3d Dupont Hospital for Children , 597 F. Plaintiffs Legal Committee , 531 U.S. 341 (2001). 2023 WL 7019287, at *7.

Fraud 52

Fraud FDA Hospitals Doctors 52

Drug & Device Law

OCTOBER 23, 2023

312 (2008), that essentially all product liability claims against manufacturers of FDA pre-market approved (“PMA”) medical devices were preempted. Elizabeth’s Hospital of Chicago, Inc. , 2004); Sheetz v. 2004) (Posner, J.); Back in 2008, the United States Supreme Court held, in Riegel v. Medtronic, Inc. , 2d 1, 11 (Ill.

FDA 59

FDA Governance Nurses Hospitals 59

Drug & Device Law

JANUARY 15, 2024

We have discussed how exclusion of FDA compliance in pelvic mesh cases, based on a false equivalence between preemption and evidentiary admissibility, has hampered the defense in that litigation. In state court, Creazzo remains binding precedent. Central Medical Health Services, Inc. , 2d 521 (Pa. 3d 1245 (N.J.

Compliance 52

Compliance FDA Governance State Policy 52