Device Vigilance
We monitor your products performance post market, manage recalls and adverse event reporting, and ensure continued compliance.
Medical device safety doesn’t stop after approval. Ongoing vigilance is critical to maintaining compliance and ensuring patient safety. CARSL Consulting offers a comprehensive range of device vigilance services, including:
- Adverse Event Reporting: Ensure swift and compliant handling of device-related incidents.
- Post-Market Surveillance: Monitor your device’s safety and performance over its lifecycle.
- Regulatory Updates: Stay informed and compliant with the evolving post market vigilance requirements under the proposed Medical Products Bill.
Partner with us to manage your device vigilance responsibilities with ease and confidence.