Blog Articles

Title: Beware of Fraudulent Coronavirus Tests, Vaccines, and Treatments: FDA Issues Warning Summary:In the ongoing battle against COVID-19, the U.S. Food and Drug Administration (FDA) warns the public about the dangers of fraudulent products claiming to diagnose, treat, or prevent the virus. Some individuals and companies are exploiting the pandemic to sell unproven and illegally marketed items that can pose serious health risks.

Title: Navigating Physician Employment Contracts: Key Strategies and Pitfalls to Avoid In an era where physicians are increasingly choosing employed-model opportunities, and standardized contracts are becoming more prevalent, it might seem like negotiating contract terms is a diminishing practice. However, experts caution against this belief, emphasizing the crucial role employment contracts play in shaping a physician’s career and personal life.

Title: Surge in Physician Employment by Health Systems and Corporations Threatens Independent Practices Summary:A recent study sponsored by the Physicians Advocacy Institute reveals that 74% of U.S. physicians are now employed by hospitals, health systems, or corporate entities as of January 1, 2022, marking a significant increase from the previous year’s 69%.

Summary: Clarinetist Boja Kragulj, known for her performances in orchestras in Philadelphia and New York, has filed a $10 million lawsuit against Manhattan dentist Martha Cortes, alleging a botched dental procedure that could lead to irreversible bone loss and premature aging. Kragulj sought an alternative to double jaw surgery for lifelong dental and breathing issues and turned to Cortes in 2013.

Summary: Counterfeit medical devices are posing a growing threat in the field of aesthetic medicine, with a particular focus on devices from reputable manufacturers like Zeltiq, Inc. and Ulthera. In an article published in the September 2014 issue of Lasers in Surgery and Medicine, physicians Brian S. Biesman and Neelam Patel highlight the dangers associated with these fake devices.

Direct-to-consumer (DTC) advertising of prescription drugs has become a prominent force in the healthcare landscape, with both positive and negative implications for patients and physicians. A 2004 Food and Drug Administration (FDA) survey, part of a series exploring the effects of DTC promotion, sheds light on the dynamics between patients, healthcare providers, and pharmaceutical marketing. Traditionally, drug manufacturers directed their promotional efforts exclusively towards healthcare professionals.

Title: “Physicians Beware: Liability Risks in Purchasing Imported Drugs and Medical Devices” Summary: Physicians are facing increased legal scrutiny and liability for purchasing foreign prescription drugs and medical devices not approved by the FDA for use in the United States. Recent civil False Claims Act settlements and criminal convictions highlight the risks associated with obtaining drugs from Canada and other countries or unauthorized suppliers.

A new report emphasizes the urgent need to address patient safety as a national priority, asserting that preventable medical errors are likely the third leading cause of death in the United States. The report, released by a presidential panel called the Working Group on Patient Safety, recommends key actions to tackle “never” events, enhance transparency and data utilization, advance research, and appoint a national patient safety coordinator.

Summary: In the ever-evolving landscape of medical technology (MedTech), patient safety is undergoing a transformation from a passive assurance to a strategic imperative. Traditionally, the industry has relied on the safety and effectiveness of its products as the primary measure, but recent trends indicate a shift that demands a proactive approach.

Title: Unraveling Medical Device and Equipment Fraud: A Deep Dive into Common Schemes and Successful Prosecutions Summary: The article delves into the world of medical device and equipment fraud, shedding light on various schemes that defraud government health care programs and compromise patient safety. The Federal Food and Drug Administration (FDA) mandates registration, compliance with control requirements, and incident reporting for all medical product manufacturers.