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Webinar: How to choose the right immune-humanized platform

Drug Discovery World

These immune-humanized platforms enable researchers to test a wide range of human-specific therapeutic approaches developed to either up or down regulate immune function. The post Webinar: How to choose the right immune-humanized platform appeared first on Drug Discovery World (DDW). which is supported by The Jackson Laboratory.

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HP&M’s Larry Houck A Panelist in FDLI’s Marijuana Rescheduling Webinar

FDA Law Blog: Biosimilars

Director Larry Houck will participate as a panelist focusing on this timely topic in the Food and Drug Law Institute’s (“FDLI’s”) “High Time for a Change: Implications of DEA’s Proposed Marijuana Rescheduling” webinar June 12, 2024, 2:00-3:30 pm ET. Information and registration is available at the conference webpage here.

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Webinar: Learn how to improve cell line development

Drug Discovery World

Cell line development is labour intensive, time consuming and costly and is subject to stringent regulations to ensure patient safety. The post Webinar: Learn how to improve cell line development appeared first on Drug Discovery World (DDW). Dr Jonathan H Dempsey. About the application picodroplet technology for single cell analysis.

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Article EMA Thank You What we expect European regulators to do in June 2024

Agency IQ

What we expect European regulators to do in June 2024 In this recurring feature, AgencyIQ, through public data and previous analysis, determines what European medicine and device regulators will likely do in the month ahead, including key deadlines, meetings, events, planned regulations, comment periods, and more.

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HIPAA-Ready and Personalized Healthcare Experiences Webinar

Perficient: Drug Development

Learn about Adobe’s commitment to maintaining HIPAA-ready standards within commerce solutions and join Perficient and Adobe for a webinar hosted by CMSWire. EST Secure Digital Conversion: Unveiling Adobe’s HIPAA-Ready Commerce Solution webinar hosted by CMSWire. Thursday, February 22 at 12:00 P.M.

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Article EMA Thank You What we expect European regulators to do in May 2024

Agency IQ

What we expect European regulators to do in May 2024 In this recurring feature, AgencyIQ, through public data and previous analysis, determines what European medicine and device regulators will likely do in the month ahead, including key deadlines, meetings, events, planned regulations, comment periods, and more.

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Article EMA Thank You British regulators tease new device regulations in informative live session

Agency IQ

British regulators tease new device regulations in informative live session This week, the British regulator MHRA offered a new peek into its planned medical device regulations. BY COREY JASEPH, MS, RAC | MAR 5, 2024 11:10 PM CST Quick background on medical device regulation in the U.K. post-market regulation here.]