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Websites targeting keyword fda cdrh

5 websites are using keyword fda cdrh in their content.

 
Total results: 5
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Home | Society of Quality Assurance
http://portalrankings.com/info/sqa.org
Society of Quality Assurance - Promoting Quality in the Regulated Research Community
  • Google Analytics code: 8494204-1
  • Updated On (Date): 2012-Aug-06
  • Expiration time: 2017-Nov-04
  • Website Registered On (Date): 1997-Nov-05
Validatedsoftware - Developement and Validation for Safety Critical Embedded Devices.
http://portalrankings.com/info/validatedsoftware.com
Embedded Software Validation Solutions for Safety-Critical Certification to Standards: RTCA DO-178C / DO-278Aand EUROCAE ED-12B /ED-109), Medical (FDA/CDRH 510(k and PMA, ISO-14971, IEC 60601 / IEC 61508 / 62304, Industrial IEC 61508 and Transportation and Rail systems IEC 62679, EN-50128, IEC 61508, 49CFR236 Subpart H
  • Google Analytics code: 856241-1
  • Updated On (Date): 2017-Aug-07
  • Expiration time: 2020-Aug-09
  • Website Registered On (Date): 1999-Aug-09
Laser Compliance® Inc. - Regulations, penalties, and how we can help
http://portalrankings.com/info/lasercompliance.com
CDRH consulting, Laser CDRH, Laser Compliance®, Laser FDA, Laser IEC, Laser Legal, Laser Product Safety, Laser sales, US laser laws, laser CDRH consulting, laser Class, laser US Customs, laser approval, laser certification, laser import, laser importing, laser impound, laser inspection, laser laws, laser license, laser product compliance, laser product consulting, laser radiation, laser recall, laser safety, laser safety consulting, laser testing, Utah, Goverment
  • Updated On (Date): 2015-Aug-08
  • Expiration time: 2019-May-22
  • Website Registered On (Date): 2002-May-22
FDA 510(k) Submission Consulting and Approval
http://portalrankings.com/info/fda510k.com
FDA 510(k) consulting for medical device submission and CDRH clearance. Learn about the FDA approval and the pre-market notification 510(k) submission process.
  • Google+ User ID: 106712623764068022575
  • Google Analytics code: 1167734-1
  • Updated On (Date): 2017-Nov-16
  • Expiration time: 2023-Jan-02
  • Website Registered On (Date): 2005-Jul-20
Spiritus Partners post-market surveillance and adverse event analytics, compliance reporting and consulting for medical device manufacturers and healthcare providers
http://portalrankings.com/info/spirituspartners.com
Hospitals, healthcare systems, and medical device manufacturers post-market surveillance, adverse event analytics, compliance reporting and consulting to improve patient safety and reduce risks and costs of quality events across the supply chain. Addresses FDA, CDRH and EU MDR regulatory requirements for quality management systems and recalls
  • Updated On (Date): 2017-Oct-17
  • Expiration time: 2019-Oct-16
  • Website Registered On (Date): 2015-Oct-16
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