The International Organization for Standardization (ISO) is preparing a revision of ISO 10993-1, the critical standard governing the biological evaluation of medical devices. This update
The European Health Data Space (EHDS) Regulation was published in the Official Journal of the European Union on 5 March 2025 and will enter into
South Korea’s Ministry of Food and Drug Safety (MFDS) announced on January 24th that it has released the first-ever guidelines for the approval and assessment
In a move that has taken many in the technology and legal sectors by surprise, the European Commission has withdrawn its proposed AI Liability Directive
On Wednesday, the International Medical Device Regulators Forum (IMDRF) finalized two highly anticipated technical documents outlining guiding principles for good machine learning practices (GMLP) and
FDA Recognizes CVSS v4.0.Here’s What You Need to Know FDA Recognizes CVSS v4.0.Here’s What You Need to Know The U.S. FDA (Food and Drug Administration)
On January 7, 2025, the MDCG 2023-3, a guidance document from the Medical Device Coordination Group (MDCG) of the European Union, was updated to Revision
The United States Food and Drug Administration (FDA) released a draft guidance document on January 6, 2025, outlining its recommendations to facilitate the development and
Today marks a milestone for the EU as the AI Act enters into force after three years of development. The EU leads as the first to establish a robust AI regulatory framework. With the countdown for implementation beginning, let’s explore the timelines ahead.
Today marks a milestone for the EU as the AI Act enters into force after three years of development. The EU leads as the first to establish a robust AI regulatory framework. With the countdown for implementation beginning, let’s explore the timelines ahead.
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