“I’ve been very very very close with my audience, but when you have hundreds of millions of views every single month, it’s just not humanly possible to speak to every single viewer,” says Marjorie, who posts over 250 pieces of content to Snapchat every day. doppelgänger as a promising way to level up her career as an influencer. Though CarynAI has only been charging users for a week in beta testing, it’s already generated $71,610 in revenue from her 99% male partners, according to an income statement Marjorie’s business manager shared with Fortune. “You can have limitless possible reactions with CarynAI-so anything is truly possible with conversation.” “Whether you need somebody to be comforting or loving, or you just want to rant about something that happened at school or at work, CarynAI will always be there for you,” says the real Marjorie when we talk on the phone. On Tuesday, CarynAI will launch out of beta, and Marjorie will begin promoting across her socials where she has millions of followers. technology that has wowed, and worried, the world over the past few months. The result, CarynAI, is a voice-based chatbot that bills itself as a virtual girlfriend, with a voice and personality close enough to that of human Marjorie that people are willing to pay $1 per minute for a relationship with the bot.ĬarynAI, which launched as a private, invite-only beta test on the Telegram app earlier in May, is the latest example of the stunning advances in A.I. In its Warning Letter, the FDA acknowledged that the company has hired a consultant to address these issues.These boyfriends are dating a virtual version of Marjorie, powered by the latest artificial intelligence technology and thousands of hours of recordings of the real Marjorie.
With respect its OOS investigations, the FDA is requiring the company to provide a retrospective, third-party review of all invalidated OOS (including in-process and release/stability testing) results for products currently in the US market and within expiry as of the date of the Warning Letter and a report summarizing the findings of the analysis, including specific details for each OOS. With respect to process validation, the agency is requiring the company to provide: (1) a detailed summary of its validation program for ensuring a state of control throughout the product lifecycle, along with associated procedures (2) a timeline for performing appropriate process performance qualification for each of its marketed drug products and (3) a review of all data that supports its process validation for commercially distributed drug products. The FDA is requiring the company to take several actions. The agency said that multiple OOS investigations were closed without assignable root cause or lacked adequate scientific justification for root cause and that the company disregarded initial failing OOS results and released batches based on retested results. The agency also said in its Warning Letter that the company’s investigations into out-of-specification (OOS) testing results were inadequate. The agency said that several PV batches using a new alternate API were manufactured for losartan potassium tablets USP 50 mg and USP 100 mg without appropriately following the company’s protocol. Specifically, the FDA cited the company for not appropriately following its written and approved process validation (PV) protocol that required quality attributes to be met for three consecutive batches to qualify an alternate active pharmaceutical ingredient (API). The Warning Letter follows the FDA’s inspection of the facility from April 8 to 16, 2019 and outlines several manufacturing violations, including failure to follow written procedures for production and process control and failure to adequately investigate batch discrepancies.
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Torrent manufactures losartan potassium tablets and has been one subject of an ongoing global investigation into nitrosamine impurities in angiotensin II receptor blockers, such as valsartan, losartan and irbesartan. The US Food and Drug Administration (FDA) has posted a Warning Letter to Torrent Pharmaceuticals in Ahmedabad, Gujarat, India for several manufacturing violations at its facility in Taluka-Kadi, Indrad, Gujarat, India.
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