Activities

Regulations & Standards

DITTA supports activities that aim at regulatory convergence at international level. We contribute to efficient policies and regulations that promote innovation for the benefit of both the citizens, patients and healthcare providers.

DITTA supports activities that aim at regulatory convergence at international level. We contribute to efficient policies and regulations that promote innovation for the benefit of both the citizens, patients and healthcare providers. DITTA is leading industry efforts to promote global convergence of medical device regulations in collaboration with regulators in IMDRF and AHWP.

In addition, DITTA supports leveraging the benefits of international standards to support smart regulations – through our regional member associations and direct liaisons to relevant ISO and IEC Technical Committees.

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Cybersecurity

Clinical Evaluation

Medical Software & Artificial Intelligence

Digital health & cybersecurity

Good refurbishment practice

Environmental policy

Medical device single audit program

Standardisation

Unique Device Identification

Regulated Product Submission

Regulations & Standards

Global Health