Regulatory compliance doesn’t end once your medical device enters the market. Sponsors are required to continuously monitor product performance, manage complaints, report adverse events, and maintain up-to-date documentation to stay compliant and audit-ready.

At CMS SciDoc, we help TGA sponsors manage post-market requirements with confidence. Our support includes:

• Adverse event and vigilance reporting (MDR)
• Complaint handling processes
• CAPA management
• Post-Market Surveillance (PMS) documentation
• Annual reporting obligations
• Technical documentation maintenance
• Ongoing regulatory compliance support

Let our experts simplify your post-market compliance workload and reduce regulatory risk.

Book a free consultation with CMS SciDoc today and stay ahead of your obligations.