China Regulatory Consulting for Medical Device

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. Be Aware of CFD.

OVERVIEW

This web page cirs-md.com currently has an average traffic ranking of zero (the smaller the better). We have probed twenty pages inside the site cirs-md.com and found five websites linking to cirs-md.com. There are one public network accounts owned by this website.
Pages Crawled
20
Links to this site
5
Social Links
1

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LINKS TO WEB SITE

杭州瑞旭科技集团有限公司

2018-02-12 - 瑞旭技术参加ChemCon The Americas 2018.

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

Chemical Inspection and Regulation Service Enabling Chemical Compliance for A Safer World CIRS. ECHA Announced that Completeness Check Period will be Extended from April, 2018. The Amended K-REACH will be Adopted on 20 March. A Summary of the Latest Updates of Cosmetic Regulations in China since 2017. 4 Substances are Available for CLH Consultation.

WHAT DOES CIRS-MD.COM LOOK LIKE?

Desktop Screenshot of cirs-md.com Mobile Screenshot of cirs-md.com Tablet Screenshot of cirs-md.com

CIRS-MD.COM HOST

Our parsers discovered that a single page on cirs-md.com took two thousand two hundred and eighty-one milliseconds to download. I could not detect a SSL certificate, so our web crawlers consider cirs-md.com not secure.
Load time
2.281 secs
SSL
NOT SECURE
Internet Protocol
112.124.72.90

SERVER OS AND ENCODING

I caught that this website is utilizing the Microsoft-IIS/6.0 operating system.

PAGE TITLE

China Regulatory Consulting for Medical Device

DESCRIPTION

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. Be Aware of CFD.

CONTENT

This web page cirs-md.com states the following, "China Regulatory Consulting for Medical Device." We saw that the website also said " Medical Device Registration and Approval." It also said " Manufacturing and Distributing License Approval. China Medical Device Regulatory Assistant Program MDRAP. China Medical Device Regulatory Database CMDRD. Applicable Standards and Technical Requirements. Qualified Testing Institutes in China."

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