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Online Resumes with "Investigational Device Exemption Program Coordinator"
Clinical Regulatory Affairs
Tags for this Online Resume: Management, Consulting, Quality, Quality Assurance, Quality Management, Surgical, Test, Regulatory Affairs, Advertising, Assessments
Clinical Regulatory Affairs - 0 Years of Experience
Skilled medical device regulatory affairs professional with extensive experience in quality assurance and clinical trial management, including Class III implantables and PMA devices. Six years with the FDA's Office of Device Evaluation. * Domestic and international regulatory affairs experience with a wide variety of devices ranging from disposables to Class III implants * Experienced in Quality System development
Tags for this Online Resume: Management, Consulting, Quality, Quality Assurance, Quality Management, Surgical, Test, Regulatory Affairs, Advertising, Assessments
