Omslagafbeelding van de show DarshanTalks Podcast

DarshanTalks Podcast

Podcast door Darshan Kulkarni

Engels

Technologie en Wetenschap

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Over DarshanTalks Podcast

Welcome to DarshanTalks! We demystify fraud for legal, regulatory, and compliance essentials in the life sciences and pharmacy industries. Through engaging 15-30-minute interviews with influential change makers, short educational regulatory defbriefs, and 60 second audio takeaways, we unveil the strategies behind bringing drugs and devices to market—and keeping them there! Powered By The Kulkarni Law Firm -  Helping regulators see your business the way you do. We focus on life science issues involving medical affairs, marketing and advertising, and clinical research so that you can learn about the industry, enhance your business and grow your career.

Alle afleveringen

345 afleveringen

aflevering Unlicensed Medical Advice & The Legal Battle Over Character.AI artwork

Unlicensed Medical Advice & The Legal Battle Over Character.AI

Send us Fan Mail [https://www.buzzsprout.com/2239432/fan_mail/new] What happens when an artificial intelligence chatbot generates a fake medical license number and starts giving psychiatric advice? In this episode of the KF Deep Dive, host Darshan welcomes healthcare regulatory expert and Fox Rothschild Chief Privacy Officer, Elizabeth Litten, to untangle a wild new frontier in legal tech. We break down the historic lawsuit filed by Pennsylvania Governor Josh Shapiro against Character.AI after a companion bot unlawfully held itself out as a licensed physician. Darshan and Elizabeth pull back the curtain on the critical compliance flaws of generative AI in healthcare. From the "overwarning" dilemma in Electronic Medical Record (EMR) systems to the dangerous lack of human oversight and clinical judgment, this conversation highlights why letting AI act as a "black box" diagnostic tool is a massive liability risk. Tune in as they discuss: * The Character.AI Lawsuit: Why the state of Pennsylvania is cracking down on AI bots posing as licensed mental health professionals. * The "Level 1" Error Problem: How software developers shift malpractice liability onto clinicians by forcing endless, low-level warning click-throughs. * Consent & The Ambient AI Trap: The hidden dangers of data-scraping, the illegality of selling Protected Health Information (PHI) under HIPAA, and why doctors must get explicit patient consent before using AI note-taking tools. * AI Governance Guidelines: Elizabeth’s top 3 compliance strategies for companies looking to safely deploy AI characters and automated tools without facing massive legal repercussions. Whether you are a healthcare professional, a software developer, or just fascinated by the intersection of law and cutting-edge technology, this episode is a must-listen guide to navigating the untamed wild west of AI. Support the show [https://www.buzzsprout.com/2239432/support] www.kulkarnilawfirm.com

18 mei 2026 - 15 min
aflevering Sponsoring Cannabis Research artwork

Sponsoring Cannabis Research

Send us Fan Mail [https://www.buzzsprout.com/2239432/fan_mail/new]  NOT LEGAL ADVICE  For decades, cannabis research in the U.S. was stifled by Schedule I restrictions, requiring high-security vaults, mountains of paperwork, and extremely limited supply chains. With Executive Order 14370, the landscape has shifted. Marijuana is moving to Schedule III, and the rules of the game have officially changed. In this episode of KLF Deep Dive, attorney-pharmacist Darshan Kulkarni breaks down the practical impact of this reclassification for clinical trial sponsors. We move beyond the headlines to discuss the "pharmacy-style" compliance now required and the hidden pitfalls of using non-pharmacist staff at trial sites. Key Topics Covered: * The Security Shift: Why you can ditch the steel vaults, but why your new "pharmacy" status brings a different set of DEA headaches. * Supply Chain Normalization: Moving away from the "one-plant" monopoly toward a traditional pharma infrastructure. * The Real-World Evidence (RWE) Invitation: How the FDA is encouraging the use of patient records and "real-world stories" to prove efficacy. * The Compliance Trap: Why vetting your trial sites’ staffing—specifically the use of CRNAs vs. Pharmacists—is now a top-tier regulatory risk. * Targeting Federal Grants: Why studies focusing on veterans and the elderly are currently "first in line" for federal support. The Bottom Line: The federal government has moved from stopping research to starting it. But as a sponsor, your site list just got bigger—and so did your responsibility to ensure they aren't just pretending to be compliant. Support the show: www.kulkarnilawfirm.com [http://www.kulkarnilawfirm.com] Support the show [https://www.buzzsprout.com/2239432/support] www.kulkarnilawfirm.com

6 mei 2026 - 4 min
aflevering Why Private Membership Associations Fail FDA Scrutiny artwork

Why Private Membership Associations Fail FDA Scrutiny

Send us Fan Mail [https://www.buzzsprout.com/2239432/fan_mail/new]  In this episode of the KLF Deep Dive, Darshan Kulkarni deconstructs a persistent and dangerous myth circulating in life sciences and investment circles: the Private Membership Association (PMA). While often marketed as a "contract-based loophole" to evade FDA oversight and civil liability, the reality in federal court is starkly different. Darshan examines the constitutional limits of "freedom of association" and analyzes key case law—including Little v. Q Lasers—to demonstrate why PMAs are viewed by judges as red flags rather than legal shields. If you are advising clients on regulatory shortcuts, this is a must-listen briefing on maintaining professional integrity and statutory compliance.  Support the show [https://www.buzzsprout.com/2239432/support] www.kulkarnilawfirm.com

16 apr 2026 - 7 min
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