Medical device regulation in Asia has gained more importance than ever. Governments and regulatory bodies across the region have put in place new regulatory systems or refined the existing ones. A registered product requires a lot of technical documentation to prove its efficacy, safety, and quality. A smooth and successful registration process demands soft skills for dealing with various key stakeholders in the government, testing centers, and hospitals and among doctors.
Handbook of Medical Device Regulatory Affairs in Asia covers medical device regulatory systems in different...
Medical device regulation in Asia has gained more importance than ever. Governments and regulatory bodies across the region have put in place new r...
