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  • stemart

Safety System Services In Usa California

5 services found
In CaliforniaAvailable In CaliforniaNear California

Combination Product Development

Combination Product Development

Manufactured by:ZebraSci Inc.   based inTemecula, CALIFORNIA (USA)
ZebraSci’s experience in primary container engineering, human factors, and medical device commercialization for auto-injectors, needle safety devices and novel drug-device systems assists organizations in developing combination products – from early concept through commercial launch and post-market ...
CONTACT SUPPLIER

Onda - Regulatory Measurements Services

Onda - Regulatory Measurements Services

Manufactured by:Onda Corporation   based inSunnyvale, CALIFORNIA (USA)
We provide general guidance, reporting, and measurements services for regulatory measurements in accordance with the IEC 60601 series ...
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Chemical, Biological, and Radiological Defense Services

Chemical, Biological, and Radiological Defense Services

by:Integrated Science Solutions, Inc   based inWalnut Creek, CALIFORNIA (USA)
As a member of the design team for a BSL-3 chemical and biological warfare agent laboratory, ISSi developed a comprehensive risk assessment, including agent analysis, and a system safety ...
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Platform and Interoperability

Platform and Interoperability

Manufactured by:Omnicell   based inSanta Clara, CALIFORNIA (USA)
Connective pharmacy automation technology to unleash full potential. Healthcare leaders and clinicians need pharmacy technology that simplifies operations instead of complicating them. This is achieved when your systems are integrated and interoperable. Omnicell solutions connect the pharmacy ecosystem by surfacing real-time data insights, streamlining pharmacy business, and enabling new ...
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STEMart - Notified Body (EU) Services

STEMart - Notified Body (EU) Services

by:STEMart   based inShirley, CALIFORNIA (USA)
CE marking is the manufacturer's declaration that their product complies technically and administratively with the essential regulatory requirements of Medical Device Directive 93/42/EEC (MDD) and its supplementary Directive 2007/47/EEC, Active Implantable Medical Devices Directive 90/385/EEC (AIMDD) and In Vitro Diagnostics Directive (IVDD) 98/79/EC, which outline the safety and performance ...
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