ComplianceOnline

Expert Profile


Ginette M Collazo
Organizational Psychologist, Ginette M Collazo Inc

Ginette Collazo, PH.D, is a human error and human behavior expert. She has spent more than 15 years in technical training, organizational development and human reliability areas. She has worked with Bristol-Myers Squibb, Johnson & Johnson, Schering-Plough, Wyeth, and has been a consultant with major firms like Abbott, Johnson & Johnson, Perrigo, among many others. She has also implemented human error reduction programs and technology in many small and mid-sized drug and device companies. An active researcher in specialized studies related to human reliability, she is the author of numerous publications on these topics.

Trainings by Expert

Human Error Reduction in GMP Manufacturing
Category: Drugs and Chemicals (Pharma) , Risk Management , All FDA Regulated Industry , Hitech, Aerospace and Manufacturing , Quality Management , Food Safety Compliance , Quality and Safety , Quality & Safety , CPG & RETAIL , Food & Dietary Supplements , Manufacturing & Contamination control , Best practices , Tools and techniques , Manufacturing Quality , Quality management tools , Food Safety & Quality , Life sciences QA/QC , Compliance & Ethics , Supply chain & Procurement , Regulations & Guidances , Best Practices & GXPs , Life Sciences , ISO 22000 , HACCP , QA/QC

How to Write Error Free and FDA Compliant Procedures
Category: Drugs and Chemicals (Pharma) , Medical Devices , Laboratory Compliance , All FDA Regulated Industry , FDA 21 CFR Part 11 , Documentation and IT , Quality and Safety , Drugs Regulations , Clinical Trial Regulations , Biotech Regulations , Documentation and Policy Management , Lifescience process & Procedures , Life sciences QA/QC , Regulations & Guidances , Life Sciences , Regulatory Affairs , Common FDA Regulations , QA/QC

Human Error and Cognitive Load: How to Reduce Memory and Attention Failures
Category: Drugs and Chemicals (Pharma) , Medical Devices , Biotechnology , Laboratory Compliance , All FDA Regulated Industry , GXP Pharmaceutical , GXP Medical Devices , Quality and Safety , Supply Chain and Manufacturing , Laboratory , Quality & Safety , OSHA Regulations , Drugs Regulations , Biotech Regulations , Risk Management & Controls , All FDA Regulated Functions , Life sciences QA/QC , Regulations & Guidances , Best Practices & GXPs , Life Sciences , Regulatory Affairs , Common FDA Regulations , QA/QC

Human Error Investigations, Root Cause Determination and CAPA Effectiveness
Category: Drugs and Chemicals (Pharma) , Medical Devices , Biotechnology , Laboratory Compliance , All FDA Regulated Industry , Quality and Safety , QMS, ISO 13485, CAPA , Supply Chain and Manufacturing , Laboratory , Quality & Safety , Drugs Regulations , Biotech Regulations , Life sciences QA/QC , Regulations & Guidances , Life Sciences , Regulatory Affairs , QA/QC

Tools for Human Error Reduction
Category: Drugs and Chemicals (Pharma) , All FDA Regulated Industry , GXP Pharmaceutical , Quality and Safety , Drug Development , Drugs Regulations , Risk Management & Controls , All FDA Regulated Functions , Audit & Inspection-Role , Quality Audit , All FDA Reg. based Audit , Drugs Inspections , Documentation and Policy Management , Lifescience process & Procedures , Life sciences QA/QC , Research & Development , Drug R & D , Regulations & Guidances , Best Practices & GXPs , Life Sciences , Regulatory Affairs , Common FDA Regulations , QA/QC

Creating and Maintaining an Effective and Efficient Technical Training Programs
Category: Drugs and Chemicals (Pharma) , All FDA Regulated Industry , GXP Pharmaceutical , Quality and Safety , Drug Development , Drugs Regulations , All FDA Regulated Functions , Audit & Inspection-Role , Quality Audit , All FDA Reg. based Audit , Drugs Inspections , Documentation and Policy Management , Lifescience process & Procedures , Life sciences QA/QC , Research & Development , Drug R & D , Regulations & Guidances , Best Practices & GXPs , Life Sciences , Regulatory Affairs , Common FDA Regulations , QA/QC

How to write SOP's that Avoid Human Error
Category: Drugs and Chemicals (Pharma) , Medical Devices , Biotechnology , All FDA Regulated Industry , GXP Pharmaceutical , GXP Medical Devices , Quality and Safety , Quality & Safety , Risk Management & Controls , All FDA Regulated Functions , Documentation and Policy Management , Lifescience process & Procedures , Life sciences QA/QC , Regulations & Guidances , Life Sciences , QA/QC

Reducing memory and attention failures/errors: Understanding Cognitive Load
Category: Drugs and Chemicals (Pharma)

Human Error Reduction Techniques for Floor Supervisors
Category: Drugs and Chemicals (Pharma)

How To Implement An Effective Human Error Reduction Program
Category: Drugs and Chemicals (Pharma)