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China Medical Device Regulatory Database

China Medical Device Regulatory Database

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China Medical Device Regulatory Database | cmdrd.cirs-md.com Reviews

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China Medical Device Regulatory Database

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1

Support - China Medical Device Regulatory Database

http://cmdrd.cirs-md.com/support

Description Medical Devices Regulation Support Center(MDRSC). Welcome to China Medical Devices Regulatory Supporting Center (MDRSC). MDRSC provides comprehensive medical devices regulatory support for overseas healthcare product entering into Chinese market. It is supported by CIRS medical device regulatory consulting team. The MDRSC’s primary mission is to provide a network or communication platform for all regulatory activities in China. Submit a support request online. Tel: 86 571 8720 6559. CIRS rese...

2

Standards - China Medical Device Regulatory Database

http://cmdrd.cirs-md.com/standards

Medical Devices Standard Search System(MDSSS). Please find below the search result and select the appropriate classification. Please provide your email address with your request or comments to get the practical advice. Tel: 86 571 8720 6559. Fax: 86 571 8720 6533. Email: Elaine@cirs-group.com. MDCSS-Medical Devices Classification Search System. MDCS - Medical Devices Classification System. MDSSS-Medical Devices Standard Search System. MDRGD-Medical Device Regulations and Guidance Database.

3

About CMDRD - China Medical Device Regulatory Database

http://cmdrd.cirs-md.com/about-cmdrd

The China Medical Device Regulatory Database (CMDRD) contains five sections:. Medical Devices Classification Search System. Medical Devices Classification System. Medical Device Regulations and Guidance Database. Medical Devices Standards Search System. Medical Devices Regulatory Supporting Center. Devices are those with low risk degree and for which safety and effectiveness can be ensured through routine administration. Diagnosis, prevention, monitoring, treatment or alleviation of disease;. MDCSS lists...

4

Regulations - China Medical Device Regulatory Database

http://cmdrd.cirs-md.com/regulations

Regulations for the Supervision and Administration of Medical Devices (Decree No.650 2014). Administrative Measures for Medical Device Registration (CFDA Order No. 4 2014). Administrative Measures for the Registration of In Vitro Diagnostic Reagents (CFDA Order No. 5 2014). Administrative Rules for the Instructions and Labels of Medical Devices (CFDA Order No. 6 2014). Administrative Measures for the Supervision of Medical Device Manufacturing (CFDA Order No. 7 2014). Technical Review Guiding Principles ...

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Chemical Inspection and Regulation Service | Enabling Chemical Compliance for A Safer World | CIRS

http://www.cirs-reach.com/news/Free

Hot Service on Sale. Consulting Service by Regulations. Consulting Service by Categories. CIRS Regulation Training Service. Latest News and Articles. Detailed Rules on Registration Dossier and On-site Inspection of Formula Registration of Infant Formula Milk Powder. K-REACH 239 PECs Lead Registrants have been Elected. Deadlines of the Transition Policy on Cross-Border E-Commerce (B2C) Tax Policy. China Food Contact Material Testing. Asia-Pacific Chemical Inventory Search System Formally Goes Online.

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Case Studies - Solutions & Case Studies - China Regulatory Consulting for Medical Device

http://www.cirs-md.com/solutions_and_case_studies/case_studies

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. Service@cirs-re...

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Sitemap - China Regulatory Consulting for Medical Device

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China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. Tel: 353 41 980...

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Services - China Regulatory Consulting for Medical Device

http://www.cirs-md.com/services

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. Medical Devices...

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News & Events - China Regulatory Consulting for Medical Device

http://www.cirs-md.com/news_and_events/Webinar_Latest_Regulatory_Updates_Medical_Devices_China.html

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. New submission ...

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Quality Assurance & Compliance - Services - China Regulatory Consulting for Medical Device

http://www.cirs-md.com/services/quality_assurance_and_compliance

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. On Dec, 12.

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Risk Assessment & Management - Services - China Regulatory Consulting for Medical Device

http://www.cirs-md.com/services/risk_assessment_and_management

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. Service@cirs-re...

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News & Events - China Regulatory Consulting for Medical Device

http://www.cirs-md.com/news_and_events/Webinar_Classification.html

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. This webinar fo...

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China Medical Device Regulatory Database

Medical Devices Classification Search System(MDCSS). Input product identifier and verification code;. View classification and relevant information of your product;. Input your email address. And send the search result with initial regulatory compliance proposals. To your email;. Medical Devices Classification System (MDCS). Device for body fluid transportation. Devices for alteration of blood and body fluids. Devices for medical dressing. Other general passive medical devices. Device for ionized radiation.

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