Matt Nichols joins proptech startup to scale product engineering efforts MENLO PARK, Calif.–(BUSINESS WIRE)–#inovation—Kukun, the leading proptech platform and originator of property data, home valuations, and homeowner investment solutions, announced today that Matt Nichols has been recruited from Expedia to lead product engineering. Nichols brings expertise from one of the world’s most innovative travel and […]

The post Kukun Hires Former Expedia Technology Leader as Vice President of Engineering appeared first on Fintech News.

The post FDA Guidance on Simulated-Use Human Factors Validation Testing: Data Collection appeared first on RegDesk.

The Gensyn Protocol Trustlessly Trains Neural Networks at Hyperscale with Lower Order of Magnitude of CostLinks: Gensyn website, Litepaper, CoinFund Portfolio, TechCrunch Article LinkInvestment Thesis SummarySecular...

The post FDA Guidance on Human Factors Validation Testing: Simulated Use and Participants appeared first on RegDesk.

To begin with, we will first understand QMS. Quality Management system is a structured process and procedure which covers all aspects of designing, manufacturing, structuring, risk management, product labeling, clinical data, storage and more. This Article explains QMS perspective for drug device combination for a manufacturing company. Combination product regulated by FDA Guidance. Combination product …

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A few weeks ago, California lawmakers quietly introduced SB-1326, a bill that would amend the Medicinal and Adult-Use Cannabis Regulation and Safety Act (MAUCRSA) to legalize interstate cannabis sales, notwithstanding the status of federal law. Specifically, SB-1326 would authorize the Governor to enter into an agreement with other states authorizing medicinal or adult-use commercial cannabis

The post California Might Legalize Interstate Cannabis Sales appeared first on Harris Bricken Sliwoski LLP.

The post HSA Guidance on Grouping of Medical Devices: Grouping Categories appeared first on RegDesk.

The post FDA Guidance on Elimination of Use-Related Hazards and Human Factors Validation Testing appeared first on RegDesk.

This is a post co-written with Bernard Paques, CTO of Storm Reply, and Karl Herkt, Senior Strategist at Dassault Systèmes 3DExcite. While computer vision can be crucial to industrial maintenance, manufacturing, logistics, and consumer applications, its adoption is limited by the manual creation of training datasets. The creation of labeled pictures in an industrial context […]

We're updating UploadVR's reviews system (yes, we know, again). Starting today, we're moving to a completely unscored system with four categories: Essential, Recommended, Avoid, and unlabeled reviews. More details on what this means right here:

The post FDA Guidance on IDEs for Early Feasibility Studies: an Overview appeared first on RegDesk.

This Blog speaks about harmonization of FDA QSR and ISO 13485. Those who are new to the industry probably have so many questions like How do we start? Which Regulations need to follow? what is QSMR?  To begin with, we will first understand QMS. Quality Management system covers designing, manufacturing, structuring, risk management, product labeling, …

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