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yoshihito matsumoto
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Japan JP
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miyakonojyou
yoshihito matsumoto
1-9-●●●●akao
miyak●●●●●o-shi , Miyazaki, 885-0081
Japan JP
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miyakonojyou
yoshihito matsumoto
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miyak●●●●●o-shi , Miyazaki, 885-0081
Japan JP
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Vintara ISO 13485 -- Setting the Standard in Regulatory Compliance
Vintara’s Enterprise Portal helps leaders deploy world class best practices for the manufacture and sale of medical devices. Our configurable workflow applications will drive performance and world class regulatory compliance including:. 21 CFR Part 11 compliance. 21 CFR Part 820 compliance. Learn more about our enterprise portal -. MDDplus: Cloud Computing for Medical Device Design. Now available for enterprise or Salesforce Cloud portals!
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ISO 13485 Medical Devices Certification - Compliancehelp Consulting, LLC
Are you looking for ISO 13485 Certification? We can meet your budget and get you certified in 60-90 days! Compliancehelp is a consulting firm specializing in ISO 13485 Medical Devices Management Systems. To assist organizations achieve ISO certification and compliance. We develop a fully customized quality management system based upon what you actually do and that meets your expectations, budget and timeline. Get a free quote for ISO 13485. At how simple the process is for certification. Of your own time...
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ISO 13485:2016 consulting and auditing for medical device and IVD companies. Transitioning or new to ISO 13485:2016? Trust Emergo to help you comply with the new QMS standard. How we can assist you with ISO 13485:2016 compliance. Emergo can help you implement a new quality management system or transition from ISO 13485:2003 to ISO 13485:2016. On-Site ISO 13485:2016 Training. Fixed price, on-site training at your facility, and tailored to your needs. Perfect for groups of three or more. 2500 Bee Cave Road.
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