Glenda Guest has 14 years of experience in regulated research involving medical devices and an extensive background in clinical CRO.
Clinical Trial Design for Medical Devices
Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products
Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
New Book on How to Validate a Pharmaceutical Process from CfPIE’s Dr. Steven Ostrove
CfPIE Announces New Training Course on the Regulated Medical Marijuana Business
CfPIE Improves Website Experience for Life Science Training Attendees
CfPIE Announces New Regulatory Compliance Training Course for Compound Pharmacies
CfPIE Discusses Life Sciences Training Advancements at Regulatory Conferences
New CAPA Process Course for Medical Device Professionals
Partnership with the Society for Clinical Data Management
The Center for Professional Innovation and Education (CfPIE) provides technical training for Pharmaceutical, Biotech, Medical Device and Skin/Cosmetics professionals. CfPIE offers more than 350 class sessions annually across 80 course titles in multiple formats, such as classroom, on-site and certification programs.
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