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Medical Device Makers Granted Expedited FDA Approval Often Fail to Conduct Follow-Up Research

Medical device makers are being granted expedited FDA appprovals but often failing to conduct appropriate follow-up research. Learn more from the Chicago attorneys at Lipkin & Apter.
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FDA Will Be More Aggressive in Warning about Medical Device Risks

In January 2016, the FDA announced its plans to take a more aggressive approach to informing the public on medical device safety risks. Learn more about these updates from the attorneys at Lipkin & Apter.
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Almost 50 Physicians Call for FDA to Reverse Position on Power Morcellators

Months after the FDA discouraged doctors from using power morcellators, medical professionals are still including the tool in their non-invasive procedures. Here's what you need to know about the controversial medical tool.
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Injury and Infection in Illinois Hospitals: What You Need to Know

Around 12 of every 100 hospital stays resulted in some kind of infection or preventable injury. Find how what you need to know from the personal injury attorneys at Lipkin & Apter.
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Minority Groups Underrepresented in Clinical Trials

Representation of minority groups in clinical trials is lacking, leading to biased test results. Learn more from the personal injury attorneys at Lipkin & Apter!
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FDA Regulations Lead to Uncertain Future for Pelvic Mesh

The FDA issued final orders with stricter data requirements for surgical pelvic mesh, also known as transvaginal mesh as the result of an increasing number of lawsuits. Learn more from the personal injury attorneys at Lipkin & Apter!
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