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Cannabinoids receptors: popular preclinical target but banned in 137 countries

Pharmaceutical Technology

Cannabinoid receptors fall into two categories: CB1 and CB2 receptors. Despite the current popularity of cannabinoid receptors, the regulatory landscape is challenging and complex. In the US, the world’s largest pharmaceutical market, most states have legalized cannabinoids for medical use.

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Hyman, Phelps & McNamara, P.C. Takes Top Honors in Two Prestigious Categories in 2023 LMG Life Sciences Awards

FDA Law Blog: Biosimilars

is pleased to announce it took top honors in two categories in the 2023 LMG Life Sciences Awards, which recognize the best life science practitioners and firms over the past 12 months from the United States, Canada, and Europe. The firm’s clients are as diverse as the regulatory issues they face. life sciences industry.

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Informa Connect’s Health Systems & Pharma Partnering Summit

Drug Channels

Cannot be combined with special category rates or other offers. Drug Channels readers will save 10% off when they use code 23DRCH10 and register prior to July 28, 2023.* * Cannot be combined with other offers or used towards a current registration. Other restrictions may apply. Drug Channels, or any of its employees.

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Informa Connect’s PBM Contracting Summit

Drug Channels

Cannot be combined with special category rates or other offers. Drug Channels readers will save 10% off when they use code 23DRCH10 and register prior to November 10, 2023.* Other restrictions may apply. The content of Sponsored Posts does not necessarily reflect the views of Pembroke Consulting, Inc.,

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Four things you need to know about FDA regulations and digital health

pharmaphorum

Devices, like pharmaceuticals, are divided into risk categories with heavier or lighter regulation depending on the risk to the patient. You have a pacemaker on one end and a tongue depressor on the other, and then FDA has to figure out a regulatory scheme that takes into account every one of them, again, without stifling innovation.”.

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Considerations for Mobile Health Technology Developers: Part 1

pharmaphorum

If so, developers must develop and execute on a regulatory strategy. Determining whether a product is a medical device subject to FDA regulation necessarily begins with understanding the FDA regulatory definition of ‘medical device’. Food and Drug Administration (FDA) regulation as a medical device. General Wellness Products.

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Informa Connect’s Medicaid Drug Rebate Program (MDRP) Summit

Drug Channels

You'll return to the office having mastered complex regulatory guidelines to deliver compliant government pricing and reporting programs. Don’t miss the chance to conquer the complex, ever-evolving regulatory guidelines and accelerate your career by sourcing world-class content and everyone who matters in Medicaid.