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Las Vegas, Nevada Area United States
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Senior Consultant at MedTech Review, LLC
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THE RIGHT CONSULTANT MAKES A DIFFERENCE The skills to bring medical devices to market are highly specialized and dynamic. Companies can be blindsided by immediate needs they are not equipped to address – and that can be costly in both time and money. THAT'S WHY THERE IS MEDTECH REVIEW We know how to move through the gridlock of the complex regulatory, quality management and submission processes with speed and accuracy. Whether you need corrective action – like responding to a letter from the FDA—or preventive action – like a situational analysis or potential problem analysis for compliance– you need it now, and you need it right. Specialties: ce marking, china, cmdcas, fda, 483, re...
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Presentations(4)Ìý

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Electronic Submissions
Electronic SubmissionsElectronic Submissions
Electronic Submissions
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China\'s Medical Device Regulatory Process
China\'s Medical Device Regulatory ProcessChina\'s Medical Device Regulatory Process
China\'s Medical Device Regulatory Process
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Sterilization Standards Update: Strategies for Compliance
Sterilization Standards Update:  Strategies for ComplianceSterilization Standards Update:  Strategies for Compliance
Sterilization Standards Update: Strategies for Compliance
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Documents(2)Ìý

Electronic Submissions Speech
Electronic Submissions SpeechElectronic Submissions Speech
Electronic Submissions Speech
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5 Errors To Avoid When Implementing Iso 13485
5 Errors To Avoid When Implementing Iso 134855 Errors To Avoid When Implementing Iso 13485
5 Errors To Avoid When Implementing Iso 13485
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