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FDA Tightens Expectations for Biosimilar Promotion

Explore 2025 US FDA Q&A Guidance on rendering information about reference and biosimilar products in promotional labeling and advertisements.

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Regulatory Affairs Training Course

Virtual training course explains FDA regulations and expectations for content, submission, and review of INDs and NDAs.

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DIA-MHRA Global Summit

Developed in partnership with the UK’s Medicines and Healthcare products Regulatory Agency (MHRA), this inaugural gathering will showcase how the UK enables innovation across the full pathway—from early development and clinical investigation to regulation, evidence generation, and real-world adoption.

DIAのデジタルマガジン「グローバル・フォーラム」

ヘルスケア関連製品の発見、開発、規制、監督、そしてマーケティングに関するグローバルな話題や地域にフォーカスした内容を、その分野のリーダーへのインタビューや教育的イベントの話題ごとのまとめをまじえた記事で、専門的な見識・洞察を知ることができます。