Search Results for keywords:"regulatory issues"

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Search Results: keywords:"regulatory issues"

  • Type:Notice
    Citation:86 FR 9506
    Reading Time:about 7 minutes

    The Food and Drug Administration (FDA) is announcing a public advisory committee meeting for the Vaccines and Related Biological Products Advisory Committee. The committee will discuss and provide recommendations regarding the strains to be included in the influenza vaccines for the 2021-2022 flu season. The meeting will be held online on March 5, 2021, from 9 a.m. to 3:30 p.m. Eastern Time, due to the COVID-19 pandemic. Public comments can be submitted until March 4, 2021, and those received by February 24 will be shared with the committee before the meeting.

    Simple Explanation

    The FDA is having an online meeting to talk about which germs should be in the flu shots for next year. People can watch it and say what they think before the meeting happens.

  • Type:Notice
    Citation:86 FR 9512
    Reading Time:about 7 minutes

    The Food and Drug Administration (FDA) is announcing a public advisory committee meeting involving the Arthritis Advisory Committee and the Drug Safety and Risk Management Advisory Committee. This meeting, which will be held online due to COVID-19, is set for March 24-25, 2021. During the meeting, the committees will discuss a drug application by Pfizer for a treatment targeting moderate to severe osteoarthritis. The FDA has established a public docket to gather comments on regulatory issues, which will remain open until March 23, 2021.

    Simple Explanation

    The FDA is having an online meeting in March with experts who will give advice about a new drug from Pfizer to help with joint pain. They want people to share their thoughts and will keep a special place open for these comments until just before the meeting.

  • Type:Notice
    Citation:89 FR 106497
    Reading Time:about 7 minutes

    The Food and Drug Administration (FDA) is holding a virtual public advisory committee meeting on February 20, 2025. The meeting will involve discussions on the benefits and risks of using dermal fillers, including new uses such as for the decolletage area. The FDA has opened a public comment period for this meeting, with comments due by March 20, 2025. Public comments submitted by January 30, 2025, will be shared with the Committee, and the public can participate by submitting comments or making presentations during the meeting.

    Simple Explanation

    The FDA is planning to have an online meeting where people talk about special creams that make skin look smooth, and they want to hear what everyone thinks. They will listen to ideas from the public until March 20, 2025, and people can send their thoughts or even speak at the meeting.