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US FDA Punts To Congress On CBD: Rx Topics Remain Outside Political Spotlight

 
• By Michael McCaughan

FDA is formally asking Congress to weigh in on the best approach to regulate CBD in consumer products. That provides another target for legislative attention that may mean that FDA’s core drug regulatory activities stay comfortably out of the spotlight.

• Source: Shutterstock

The US Food & Drug Administration is asking Congress for help on CBD regulation in the form of legislation to create a “new pathway” for consumer products that contain cannabidiol.

“After careful review, the FDA has concluded that a new regulatory pathway for CBD is needed that balances individuals’ desire for access to CBD products with the regulatory oversight needed to manage risks,” Principal Deputy Commissioner Janet Woodcock said on 26 January

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Pink Sheet Podcast: A New Director For US FDA’s Biologics Center, Guidance Production Slowdowns

 
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US FDA Layoffs Hit Conflict-Of-Interest Screening For ODAC Meeting

 
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Safety Review Prompts EMA to Suspend Ixchiq Chikungunya Vaccine For Seniors

 
• By Neena Brizmohun

The European Medicines Agency is investigating whether Valneva’s Ixchiq is safe to use in the elderly, following reports of 17 serious adverse events, including two cases resulting in death, in people aged 62 to 89 years who received the vaccine. This follows actions by US and French authorities last month regarding Ixchiq’s use in people over 65.

Unlocking Opportunities: How To Engage With The EMA On Animal Testing Alternatives

 
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