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Physicians and Providers – Regulatory Compliance

Apr 03, 2019

Physicians Role and Responsibilities in End-of-Life Request

New Jersey residents recently gained the “right to die,” as the legislature passed the Medical Aid in Dying for the Terminally Ill Act on March 25, 2019. This act gives terminally ill New Jersey residents, who have six months or less to live, the right to request oral medication to end their life.» Read More

Nov 16, 2018

What Is the Retention Requirement for a Minor’s Medical Records in New Jersey?

In New Jersey, a physician is required to maintain treatment records for seven years from the date of the most recent entry; however, questions always arise about how long a physician must retain medical records for a minor.

The State Board of Medical Examiners does not differentiate between minor and adult patients, and simply sets a seven-year retention requirement. » Read More

Oct 26, 2018

Medical Cannabis and the NJ Prescription Monitoring Program

There is no doubt that the current administration is pushing to expand the Medical Marijuana Program (MMP) in New Jersey.  Since Gov. Murphy took office this year, the number of patients registered has doubled.  The addition of five qualifying debilitating conditions and medical marijuana being viewed as a means to combat the opioid epidemic, are two of the reasons for the drastic increase in patient numbers. » Read More

Oct 02, 2018

Disclosure Requirements in Non-Emergent Cases – NJ

The Out-of-Network Consumer Protection Transparency Cost Containment and Accountability Act was adopted in June 2018 and went into effect last month.  It has gotten significant attention regarding emergent or urgent services rendered to patients, and the inability of out-of-network providers and facilities to balance bill the patient. » Read More

Jul 20, 2018

New OCR Guidance Regarding Patient Authorizations for Research Purposes

Generally, when using or disclosing an individual’s Protected Health Information (“PHI”), HIPAA regulations require the covered entity to obtain an authorization from an individual, including for research purposes[1].  The Office of Civil Rights (“OCR”), the entity that enforces HIPAA compliance, recently issued guidance for situations when an entity obtains an authorization from an individual for use and disclosure of PHI for research[2], focusing on the following topics:

  • Sufficient Description – HIPAA regulations require that the authorization, in plain language, provide “a description of each purpose of the requested use or disclosure.
» Read More

Jun 11, 2018

Artificial Intelligence in Medicine – Legal Concerns

I recently wrote the article “Artificial Intelligence in Medicine – Legal Concerns” for the Onondaga County Medical Society Bulletin. The article discusses the role Artificial Intelligence (“AI”) plays in modern medicine and the legal concerns associated with it. To read the article, please click hereRead More

Jun 08, 2018

Monitoring the Temperature of Your Vaccines for Children Program Compliance

We recently wrote the article “Monitoring the Temperature of Your Vaccines for Children Program Compliance” for MDAdvantage. The article covers the requirements of the New Jersey Vaccines for Children Program; how to properly store vaccines as required by Vaccines for Children Program and the Centers for Disease Control and Prevention; how to properly monitor the minimum and maximum temperatures of vaccine storage units; and how to address a temperature excursion.» Read More

Jun 05, 2018

Governor Murphy Signs Out-of-Network Consumer Protection, Transparency, Cost Containment and Accountability Act into Law

On Friday, June 1, 2018, Governor Murphy signed into law the Out-of-Network Consumer Protection, Transparency, Cost Containment and Accountability Act, to take effect Thursday, August 30.  The bill is intended to protect patients from surprise out-of-network medical bills.

Click here to read our alert to learn how this new Act will affect patients, insurance carriers, and health care providers.» Read More

May 25, 2018

Administering of Non FDA-Approved, Foreign Drugs Results in Criminal Conviction and Payment for False Claims Act Violation

In a recent press release, the United States Attorney’s Office for the Northern District of New York announced that a Poughkeepsie physician and his wife were sentenced for a misdemeanor for ordering and administering to patients, drugs that were not approved by the FDA and were obtained from foreign sources. » Read More

Apr 25, 2018

New York State – OMIG Releases its Work Plan for the 2018/2019 Fiscal Year

The Office of the Medicaid Inspector General (“OMIG”) has released its Work Plan for the next Fiscal Year, which encompasses April 1, 2018, through March 31, 2019.  The stated mission of the OMIG, an independent entity created within the New York State Department of Health, is to detect and prevent fraudulent practices within the Medicaid system and recover funds deemed improperly paid to health care providers. » Read More

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