Latest Guidebook for Conducting Medical Device Clinical Evaluation and Clinical Trial in China: From Regulations to Practices (2014 Edition)

DUBLIN, October 17, 2014 /PRNewswire/ --

Dublin - Research and Markets (http://www.researchandmarkets.com/research/6cbkgn/latest_guidebook) has announced the addition of the "Latest Guidebook for Conducting Medical Device Clinical Evaluation and Clinical Trial in China: From Regulations to Practices (2014 Edition)" report to their offering.

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China's regulatory framework for medical devices is undergoing radical changes. The country's new leaders have recognized that the regulations for supervision and administration of medical devices are far from perfect along with rapid population growth and thriving economy over the past 30 years. 

Chinese state council issued the latest Regulations for the Supervision and Administration of Medical Devices on February 12, 2014, which has come into force as of June 1, 2014. Before long, China Food and Drug Administration (hereafter called as CFDA) issued the latest Measures for the Administration of Medical Device Registration, which has come into force as of October 1, 2014.The overseas medical devices exporting into China market are subject to administration of overall new regulations on medical device registration since October 1, 2014. 

The Chinese concept of clinical evaluation and clinical trial for medical device registration is unique, which is distinct from the clinical trial in U.S. and EU countries. How do you in compliance with the latest Chinese regulations on medical devices? How do you operate business smoothly in China? How do you conduct the clinical evaluation and clinical trial for your products exporting into the Chinese market? 

To enter such a lucrative medical device market, overseas and multinational medical device manufacturers must have a comprehensive and thorough knowledge of the latest Chinese regulations on medical device clinical evaluation and clinical trial. Otherwise, the restrictive legal requirements and approval delays eat up your development time and budget. 

Latest Guidebook for Conducting Medical Device Clinical Evaluation and Clinical Trial in China: From Regulations to Practices (2014 Edition) not only provided a comprehensive and thorough knowledge of the latest Chinese regulations on clinical evaluation and clinical trial for imported medical device registration but also introduced the practical operation how to comply with the Chinese GCP to guide you use the Chinese trial venues to keep medical device development lean and achieve a successful approval for your products entry into the Chinese medical device market. 


Key Topics Covered: 

Chapter 1 Executive Summary. 

Chapter 2 Latest Chinese Applicable Regulations for Clinical Evaluation and Clinical Trial of Medical Device Registration. 

Chapter 3 What Chinese Regulations on Medical Device Registration are Undergoing Radical Changes ---- A Comprehensive Comparative Analysis. 

Chapter 4 An Overview of Chinese Regulatory Authorities for Clinical Evaluation and Clinical Trial of Imported Medical Device Registration. 

Chapter 5 Knowledge Preparation before Conducting Clinical Evaluation and Clinical Trial for Imported Medical Device Registration. 

Chapter 6 Medical Device Classification. 

Chapter 7 Rights of Human Subjects and Every Party's Responsibilities in Clinical Trials for Imported Medical Devices. 

Chapter 8 Clinical Evaluation and Clinical Trial of Imported Medical Device Registration. 

Chapter 9 Practical Guidance for Applying for Clinical Trials of Imported Medical Device Registration. 

Chapter 10 Practical Guidance for Conducting Clinical Evaluation of Imported Medical Device Registration. 

Companies Mentioned: 

• GE
• Siemens
• Philips

For more information visit http://www.researchandmarkets.com/research/6cbkgn/latest_guidebook

Media Contact: Laura Wood , +353-1-481-1716, [email protected]

SOURCE Research and Markets