Eye on FDA 09月29日 10:49
FDA加强执法,对社交媒体广告采取行动
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美国食品药品监督管理局(FDA)的药物推广决策办公室(OPDP)连续第二次在本月和今年第三次发布通知,表示已采取执法行动。本周OPDP通过致一家公司关于付费社交媒体发布的无标题信(UNL)采取了行动。今年FDA的执法行动在6月之前一直不存在,直到6月该机构发布了一封年度第一封信。本周的行动使得今年共发送了三封信,都在三个月内。

📌 FDA的OPDP连续多次发布通知,表示已采取执法行动,显示FDA加强了对药物推广的监管力度。

📢 本周的执法行动是通过致一家公司关于付费社交媒体发布的无标题信(UNL)进行的,涉及一种口服避孕药,该药在标签上有特定的禁忌症、警告和注意事项,以及最常见的副作用列表。

🚫 OPDP对宣传通信中的三个方面提出了质疑:在宣传中介绍适应症时没有包含风险信息;宣传中提出的声明OPDP认为没有得到包装说明书临床研究部分的支持;宣传没有按照FDA-2253表格提交审查。

For the second time this month and the third time this year, FDA’s OPDP has posted notice that it has taken an enforcement action. Last week, a Warning Letter was posted regarding a sales aid. This week it action came in the form of an Untitled Letter (NOV) sent to a company regarding a paid social media posting. Enforcement this year was non-existent until June when the agency posted its first letter in a year. This week’s action makes a total of three letters sent this year, all within a three-month period.

The Untitled Letter posted this week involved an oral birth control pill which has a specific of contraindications contained in the label as well as a list of warnings and precautions and of the most common adverse events. The communications vehicle in question was a social media sponsored posting.

OPDP took issue with three specific aspects of the promotional communication. First, while presenting the indication in the posting, there was no risk information included in the communication. Second, a claim was made in the communication that OPDP said was not supported by the clinical studies section of the package insert. And third, the communication was not submitted under form FDA-2253 for review.

It would seem that the omission of any risk information combined with the review issue would have been enough to trigger action by OPDP. But as discussed last week, previous to this letter there were four letters in a row that held efficacy claims up against studies that might support the claims and found them wanting. This is now the fifth letter in a row that took issue with an efficacy claim with OPDP scrutiny of the underlying data that may or may not exist to support the claim. Pharma communicators take note.

Last year the agency only issued a total of four letters. Enforcement trends are impossible to predict but certainly it has picked up and there could be more to come. After all, back in 2016, the agency issued six letters in the month of December alone. Stay tuned.

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FDA OPDP 药物推广 社交媒体广告 执法行动
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