Each quarter, Enlyte publishes its medical price index (MPI), which analyzes Enlyte’s medical bill review professional services charge data for trends specific to P&C claims. Check it out now! https://lnkd.in/gc3UkBbZ
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Among the array of services offered by Speed Medical, our fixed fee screening and pagination serves as a vital component, ensuring efficiency, accuracy, and cost-effectiveness in all of our services. Explore it with us in our latest blog post: https://lnkd.in/eKvqHwGz #pagination #medicaltreatments #medicalassessments #clinicalnegligence #medicolegal #blog #blogpost #medicalnegligence #medicallaw #legalservices
Understanding Fixed Fee Screening and Pagination
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Read the latest news and solutions for regulatory agencies in GL Solutions’ weekly newsletter. Our featured stories: · Universal Recognition Expanding in US, interview with Edward Timmons of The Knee Center · Multistate Licensure for Physicians Gains Steam · Top 10 Regulatory Stories of 2023 · Regulatory News Roundup · GL Solutions at Federation of Associations of Regulatory Boards-FARB conference · Easy Ways to Use AI Now · Use These Tools for Greater Efficiency https://bit.ly/3SoSNLk #Licensing #OccupationalLicensing #regulatory
Universal Recognition Expanding in U.S., Interview with Knee Regulatory Research Center's Ed Timmons
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Did you catch these important updates? Read them here! ⬇️ #policymonitoring #policyupdate
BCBS of Vermont releases NEW medical policy updates - April 2024. #medicalpolicy #reimbursement #marketaccess
Medical Policy Changes for April 1, 2024 - FINAL - Publication Copy 1.31.24.pdf
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🚨 As a professional in the medical device industry, navigating the world of adverse event reporting can feel overwhelming. But understanding your role is crucial to keeping patients safe and your organization compliant. 🩺 When it comes to reporting adverse events for medical devices, the responsibility falls on different parties depending on their role in the supply chain. 1. User Facilities A user facility like a hospital or nursing home, report any deaths related to a medical device to both the FDA and manufacturer within 10 work days. Serious injuries also need to be reported to the manufacturer (and FDA if the manufacturer is not known) within that same 10-day window. [§ 803.30](https://lnkd.in/e4Y-umDb)) 2. Manufacturers Manufacturers have 30 calendar days to report deaths, serious injuries, or malfunctions that could lead to such events to the FDA once they become aware. However, if remedial action is needed to prevent substantial public health risks, that timeline shrinks to just 5 work days. [§ 803.3](https://lnkd.in/epVrHfiE)), [§ 803.50](https://lnkd.in/eS3tRJhx)) 3. Importers Importers must alert the FDA and manufacturer about deaths or serious injuries within 30 calendar days of finding out. Malfunctions that could result in death or serious injury need to be reported to the manufacturer in that same 30-day timeframe. [§ 803.40](https://lnkd.in/e-xfiKrZ)) Even if a health professional or consumer not required to report, you can still submit voluntary reports about adverse events or product issues through the FDA's MedWatch program using Form FDA 3500. [§ 803.20](https://lnkd.in/ej5KEvaa)) The key is for each party to maintain records and stick to the reporting timelines laid out in 21 CFR Part 803. By understanding your role and requirements, you can help ensure proper reporting of medical device adverse events, even amidst the intricate regulatory landscape. 🧩
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Board Certified Orthopaedic Surgeon Foot and Ankle Surgery LA Magazine Top Doctor 2021, 2022, 2023, 2024
It is difficult to remove a QME from a case once selected, and typically this requires proving that the QME has acted outside of their scope or otherwise is disciplined for wrongdoing. It is really important for a QME to produce quality, justified reports to avoid disciplinary action and avoid being thrown off a case when the opinion may be unfavorable to one party or another. Ensure that you're always backed by the legal code when dealing with QME matters.
The Panel QME process is an essential tool for Workers’ Compensation physicians. It was established to eliminate “doctor shopping,” streamline evaluations, and gather substantial evidence for med-legal determinations. As a QME, adhering to the guidelines outlined by the DWC, including avoiding ex parte communications and producing reports that constitute substantial medical evidence, reduces the likelihood of being replaced.
The Replacement Panel Process for QMEs in California
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Reminder! Spark™ Aligners Weekly Webinar Series is happening Now! Hosted by Dr. Jose Franco, Spark Clinical Director and Dr. Karol Miranda, Spark Clinical Manager, the sessions will cover some of the most common topics related to aligner therapy including: 👉 March 1 Deep Bite Case Revision and Protocols 👉 March 8 Aligner Case Selection 👉 March 15 Treating Posterior Crossbite with Aligners Each session is designed to efficiently and effectively give you the knowledge you need to take your aligner skills to the next level. Since each session is just 30 minutes long, they will conveniently fit into your busy schedules. 𝗥𝗲𝗴𝗶𝘀𝘁𝗲𝗿 𝗻𝗼𝘄! https://lnkd.in/gX5pUxNc The speaker has made all efforts to support clinical recommendations with references from scientific literature whenever possible. Ormco is a medical device manufacturer and does not dispense medical advice. Clinicians should use their own professional judgment in treating their patients. Patient results may vary. #SparkAligners #AlignerTherapy #ClearAligners #Ormco #SparkAlignersWebinar
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Do you use an implantable medical device or know some one who does? NSW Health's Clinical Excellence Commission is wanting to know your experiences with the current system and to make the experience better for future clients. Let them know your thoughts on how to do this by filling in their quick survey! (See CEC's post for the survey link).
We want to hear from patients who have had an implantable medical device inserted since 2020. The survey only takes a few minutes and will ask patients how they receive information about their device(s) and their level of satisfaction with current processes. The survey is anonymous and the results will help inform the CEC’s Medical Device Governance Program. Complete the survey here: https://bit.ly/48e0Ek4 An implantable medical device is a device that is introduced into the body and remains for at least 30 days after the procedure, such as a joint replacement or pacemaker. The Therapeutic Goods Administration has introduced new reforms to strengthen the regulation of medical devices in Australia. The CEC is implementing the reforms within NSW Health. The survey has been extended to 29 February 2024. More information for patients is available on the CEC website. https://bit.ly/4aehJfs
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The process of formulating a settlement demand is time consuming. Synergy's Medical Cost Projection helps you to quantify future medical by including our report with your demand. Check out our blog that explains the standard of care and evidence based medicine guidelines that are incorporated in each report.
Damages in Personal Injury Lawsuits - Synergy
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With the recent revisions and improvements that CMS just came out with for Prior Authorizations, it's important for physicians to know as much as possible to streamline the process, and maximize the approval rates. Click below for 8 ways to Make Prior Authorizations easier! As posted by Medical Economics #thebusinessofmedicine #priorauthorization #medicalequipment #diagnostictests #medicaldiagnostics #reimbursablemedicaltools #CPT #reimbusrsabletesting #physicansoffice #physician https://lnkd.in/e2Ximwry
Make Prior Authorizations Easier
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In order to really appreciate how far medicine has come over the years, it’s worth looking back at what was once considered acceptable. Here are 5 of the craziest medical practices that were once the norm for doctors and patients around the world. #Blog #MedicalHistory #ProgressInMedicine https://lnkd.in/g6NSqX6Y
5 Crazy Medical Practices That Were Once the Norm
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