Swissmedic Guidance on Incident Reporting: Specific Aspects
The new article describes in detail certain specific aspects related to the incident reporting requirements introduced in Switzerland.
The new article describes in detail certain specific aspects related to the incident reporting requirements introduced in Switzerland.
The article highlights the key points related to the regulatory requirements in the sphere of incident reporting in the context of healthcare products allowed for marketing and use in Switzerland.
The new article elaborates on the specifics of the regulatory approach medical device software products are subject to.
The article provides an overview of the trend report template issued by the Swiss regulating authority.
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