Events Tagged "medical devices"

China Compliance Processes for Life Science

This webinar will discuss the regulatory structure and requirements for compliance with Chinese SFDA regulations for Pharmaceuticals, Medical Devices, Biologics and Combination Products.

Medical Device Adverse Event Reporting

This 3-hr virtual seminar will discuss the requirements and compliance in medical device adverse event reporting and medical device surveillance/vigilance system in the US, Europe and Canada.

Latin America: Regulatory Compliance Requirements

This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America.

Post Market Surveillance for Medical Devices

Post market surveillance is changing, not only in the US, but also in the EU and Canada.

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