Compliance doesn’t stop at market entry. As a TGA sponsor, you must actively monitor, report, and maintain the ongoing safety and performance of your medical device.

CMS SciDoc supports sponsors with end-to-end post-market compliance, including:
✔ Adverse event & vigilance reporting (MDR)
✔ Complaint handling systems
✔ CAPA management
✔ Post-Market Surveillance (PMS) documentation
✔ Annual reporting obligations
✔ Technical documentation maintenance
✔ Continuous regulatory compliance support

Be inspection-ready. Be confident. Be compliant.

👉 Book your free consultation with CMS SciDoc today. info@cmsscidoc.com