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Expert Profile


Gerry O Dell
President, Gerry O’Dell Consulting

Gerry O'Dell, is owner and President of Gerry O'Dell Consulting, a consulting firm based in the United States with medical device and pharmaceutical clients around the world. Prior to starting Gerry O'Dell Consulting, she worked for Johnson & Johnson Medical, Inc. as the Manager of Laboratory & Sterilization Services which managed the sterilization program for J&J Medical in addition to providing laboratory testing services to several J&J companies. Before becoming a part of Johnson & Johnson Medical, Gerry was Manager of Sterilization Services at Critikon, Inc where she started as a Lab Technician. She holds both a Bachelor and Master of Science degree in Microbiology from the University of South Florida and has over twenty-nine years of experience in the medical device industry.

Trainings by Expert

Ethylene Oxide (EO) Sterilization Basics for R&D Engineers
Category: Medical Devices , Laboratory Compliance , Sterilization , Life Sciences

Basics of Testing Associated with Sterilization Validation and Routine Processing
Category: Drugs and Chemicals (Pharma) , Medical Devices , FDA Validation , Sterilization , Life Sciences

You have a BI or Sterility Failure - Now What?
Category: Medical Devices , Supply Chain and Manufacturing , Life Sciences

How to Investigate Environmental Monitoring Excursions Limits
Category: Medical Devices , Supply Chain and Manufacturing , Life Sciences

Troubleshooting Ethylene Oxide (EO) Processes
Category: Medical Devices , Supply Chain and Manufacturing , Life Sciences

Designing an Effective Cleaning Validation for Reusable Medical Devices in Today's Regulatory Environment
Category: Medical Devices , Testing and Validation , Life Sciences

Compliant Supply Chain & Manufacturing for Medical Devices - Comprehensive Training Package (8 Courses)
Category: Medical Devices

You have a BI Positive or Product Sterility Positive - Now What?
Category: Medical Devices , Testing and Validation , Sterilization , QMS, ISO 13485, CAPA , R & D , Life sciences QA/QC , Research & Development , Device R & D , Life Sciences , QA/QC

Process Challenge Device Development for EO Sterilization
Category: Medical Devices , GXP Medical Devices , Sterilization , Supply Chain and Manufacturing , R & D , Life sciences QA/QC , Research & Development , Device R & D , Regulations & Guidances , Life Sciences , QA/QC

Responding to a Dose Audit Test Failure
Category: Medical Devices