Introducción a las normativas de productos sanitarios de la USFDA

abril 22, 2025 by mambani

Join Registrar Corp’s experts as they break down the fundamentals of medical device regulation in the United States. From device classification and 510(k) requirements to registration, labeling, and UDI compliance, this session is ideal for medical device companies looking to enter or expand in the U.S. market.

Únete a los expertos de Registrar Corp mientras desglosan los fundamentos de la regulación de dispositivos médicos en los Estados Unidos. Desde la clasificación de dispositivos y los requisitos 510(k) hasta el registro, el etiquetado y el cumplimiento de UDI, esta sesión es ideal para empresas de dispositivos médicos que buscan entrar o expandirse en el mercado estadounidense.

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FDA registration today.

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For more assistance with FDA regulatory requirements, call: +1-757-224-0177, email: info@registrarcorp.com, or chat with a Regulatory Advisor 24-hours a day: www.registrarcorp.com/livechat.

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