China

RegistrationPost-marketClinical TrialMedical DeviceTestingInnovativeChina AgentChina
Medical DeviceMedical Device
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🍜 China's New Risk Rules

🍜 China's New Risk Rules

NMPA Draft Could Up-Class Your Device

Elaine Tan
Medical DeviceMedical Device
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🍜 Future of Medical Device Industry in China (Part 2)

🍜 Future of Medical Device Industry in China (Part 2)

Elaine Tan
Medical DeviceMedical Device
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🍜 Future of China's Medical Device Industry (Part 1)

🍜 Future of China's Medical Device Industry (Part 1)

Elaine Tan
Medical DeviceMedical Device
+1+1
🍜 EU-China Tension Over Medical Device Procurement

🍜 EU-China Tension Over Medical Device Procurement

Elaine Tan
Medical DeviceMedical Device
+2+2
🍜A Journey of Innovative Medical Devices

🍜A Journey of Innovative Medical Devices

Elaine Tan
Clinical TrialClinical Trial
+2+2
🍜 NMPA Update: New Devices Exempt from Clinical Evaluation

🍜 NMPA Update: New Devices Exempt from Clinical Evaluation

Elaine Tan
Post-marketPost-market
+2+2
🍜 China PMS (Part 3): When Is Reassessment Needed?

🍜 China PMS (Part 3): When Is Reassessment Needed?

Elaine Tan
Post-marketPost-market
+2+2
🍜 Post-market Surveillance (Part 2)

🍜 Post-market Surveillance (Part 2)

Elaine Tan
Post-marketPost-market
+1+1
🍜 Post-market Surveillance (Part 1)

🍜 Post-market Surveillance (Part 1)

Elaine Tan
TestingTesting
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🍜 An Alternative to Accredited Laboratory Tests?

🍜 An Alternative to Accredited Laboratory Tests?

Elaine Tan
TestingTesting
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How to get your medical device tested in China

How to get your medical device tested in China

Elaine Tan
TestingTesting
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Your Blueprint to the Product Technical Requirements (PTR)

Your Blueprint to the Product Technical Requirements (PTR)

Elaine Tan