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2025 Physician Wellness Retreats | Physician “Burnout” Retreats

Pamela Wible MD

Your retreat includes: Daily spa treatments and gourmet meals delivered to your hot tub A personalized business launch plan: from fee structure to client contracts Search-engine-optimized website copy and marketing strategy 20 hours of bonus Live Your Dream Fast Track training —free! Can’t travel? Virtual retreat options available.

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Podcast: AI, innovation, and value-based care in medicine

Permanente Medicine

” Related AI scribes story: Analysis: AI scribes save physicians time, improve patient interactions and work satisfaction Dr. Nguyen also highlighted the potential to utilize artificial intelligence and Kaiser Permanente’s extensive medical database to develop predictive analytic models aimed at enhancing patient care.

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FDA Releases Final Guidance on Use of Digital Health Technologies for Remote Data Acquisition in Clinical Investigations

FDA Law Blog

Considerations for design of usability evaluation are provided as well as a statement that the principles in the FDA’s guidance on Applying Human Factors and Usability Engineering to Medical Devices may be helpful in designing appropriate usability evaluations for DHTs. By Adrienne R. investigational device as defined in 21 C.F.R.

Clinic 105
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Hearing Loss in Geriatrics and Palliative Care: A Podcast with Nick Reed and Meg Wallhagen

GeriPal

We talk with Nick and Meg about: Why hearing loss is important not just in geriatrics but also for those caring for seriously ill individuals. Communication techniques we can use when talking to individuals with hearing loss. Think about the last time you attended a talk on communication skills or goals of care discussions.

IT 102
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Mastering Responses to FDA 510(k) AI Letters: A Strategic Approach

FDA Law Blog

By Philip Won & Adrienne R. Lenz, Principal Medical Device Regulation Expert — It takes a significant amount of time, cost, and effort to prepare a premarket notification 510(k) submission. But that is only the beginning. After a firm submits a 510(k) to FDA, FDA will request still more information after a first-pass review. The stakes are high.

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OTAT Becomes the Office of Therapeutic Products (OTP) and Kicks off Town Hall Series – They appear to be tired of writing the same “Complete Response” Letters

FDA Law Blog

The standard practice is for FDA to engage with companies on an individual basis through formal meetings and deliver directed feedback to specific sponsor questions. OTP has spent years communicating industry-wide problems on an individual basis. OTP recognized that this strategy may not be possible for all products (e.g.,

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Texas invests $50M in psychedelic drug research to treat addiction

Medical Xpress

The goal is to support clinical trials and bring in another $50 million in private investment to help ibogaine win approval from the U.S. Food and Drug Administration (FDA). The process could take years. Ibogaine is made from the root of a plant found in Africa. It has been banned in the U.S. Former Texas Gov.