Since 2004, QME has dedicated itself to provide medical device registration and clinical trial service in China. We have assembled a pool of skilled technicians, regulatory specialists and clinical experts, and are capable of providing one-stop solutions for our clients. Thanks to our efforts of many years in medical device industry, we have successfully provided professional and efficient services for hundreds of manufacturers worldwide, including various renowned enterprises and leading brands. Based on our solid expertise and thorough understanding of regulations, with our customer-centric principles, we have become the most trusted partner in the industry. We are confident to be your helpful partner to develop your business in China.
Our Services
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Registration |
Clinical trial |
Consultation |
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Product Classification |
Clinical protocol design |
Regulation consultation |
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Draft & Review registration documents |
Clinical center selection |
Quality system certification |
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Product testing and technical support |
Clinical trial monitor |
Translation |
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Apply for registration & guide evaluation |
Statistical analysis and Data management |
CFDA agent |
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Follow-up all process & deliver certificates |
Clinical trial report compilation |
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Advantages:
Quicker Achievements
ü Sooner return on investment
ü One step ahead of your competitors
Minimum Cost
üBest use of existing materials
ü Least involvement of tests
Enjoyable Cooperation
ü Proactive involvement
ü Wholehearted customer care
Contact us
Beijing QME Consulting Co. Ltd.
C-602, Ruipu Building, No. 15, Hongjunying South Road, Chaoyang District, Beijing 100012
Tel: 86-10-64187881
Email: service@qiminer.com
Web：www.qiminer.com
Nice to meet you!
