Compliance Informed Consent Malpractice 
Compliancy Group
OCTOBER 21, 2024
The Health Insurance Portability and Accountability Act (HIPAA) compliance patient consent form is essential for properly using and disclosing protected health information (PHI). Failure to get informed consent can have dire consequences for your organization.
AIHC
SEPTEMBER 5, 2023
Compliance Considerations for Best Outcomes Written in collaboration with the AIHC Volunteer Education Committee Delivering mental health services via telehealth has increased since the COVID-19 pandemic. Obtaining informed consent with your patient is typically done before the first appointment.
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MedTrainer
APRIL 11, 2024
Incident reporting is essential to maintain a healthcare organization’s compliance with state and federal regulations and reveal what are the main types of healthcare incidents. billion in malpractice costs and almost 2,000 preventable deaths. MedTrainer offers all the functions listed above in an all-in-one compliance solution.
AIHC
JANUARY 5, 2022
Contact your risk attorney through your malpractice insurance company for guidance which is obtained through no additional cost (part of the service you get when paying the insurance premium). The American Medical Association (AMA) also posts helpful information for providers and offers an initial toolkit. Identify eligible cases.
Drug & Device Law
AUGUST 8, 2022
Apparently, a fraudulent foreign-trained “doctor” treated the plaintiffs, none of whom claimed malpractice or any physical injury whatsoever. Anyway, this fraudulent “doctor” allegedly “touched them without informed consent” and caused them “emotional distress. has no power to enforce compliance”), aff’d , 405 F.
Drug & Device Law
JANUARY 28, 2022
Fajardo held that Plaintiffs’ email was not in technical compliance with Connecticut rules of procedure and was especially critical of Plaintiffs for failing to cite any evidence in that email, which would have warranted a denial of their request. But anyone who has a medical malpractice defense practice will be interested in that rationale.
Drug & Device Law
JUNE 7, 2022
The last provision cited by plaintiff’s side was one that allows the fact finder to consider evidence of compliance with regulations. Doctors are charged with discussing the risks and benefits of treatment and obtaining informed consent from their patients.
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