ComplianceOnline

Expert Profile


Charles H Paul
President, C H Paul Consulting Inc

Charles H. Paul is the President of C. H. Paul Consulting, Inc. – a regulatory, training, and technical documentation consulting firm. Charles is a management consultant, instructional designer and regulatory consultant and has led C. H. Paul Consulting, Inc. since its inception over 25 years ago. He regularly consults with Fortune 500 pharmaceutical, medical device, and biotechnology firms assisting them in achieving human resource, regulatory, and operational excellence. He is a regular presenter of webinars and on-site seminars in a variety of related subjects from documentation development to establishing compliant preventive maintenance systems.

The firm works globally completing projects throughout the EU, UK, South America, and Asia.

Trainings by Expert

Risk Analysis in Medical Device Design
Category: Medical Devices , Medical Devices , Risk Management , All FDA Regulated Industry , GXP Medical Devices , Quality and Safety , Supply Chain and Manufacturing , R & D , Risk Management & Controls , All FDA Regulated Functions , Life sciences QA/QC , Research & Development , Device R & D , Regulations & Guidances , Life Sciences , Regulatory Affairs , Common FDA Regulations , QA/QC

Successful Device Submissions and Approvals - Key Elements
Category: Medical Devices

Classifying Medical Devices - US and EU
Category: Medical Devices , Packaging and Labeling , All FDA Regulated Industry , Drug and Device Approvals , Marketing and Promotion , Supply Chain and Manufacturing , Documentation and Policy Management , Lifescience process & Procedures , Regulations & Guidances , Life Sciences , Regulatory Affairs , Documentation and Data Management

Introduction to FDA and EU Medical Device Submission
Category: Medical Devices , All FDA Regulated Industry , GXP Medical Devices , Quality and Safety , QMS, ISO 13485, CAPA , Supply Chain and Manufacturing , R & D , Life sciences QA/QC , Research & Development , Device R & D , Regulations & Guidances , Best Practices & GXPs , Life Sciences , Regulatory Affairs , QA/QC

3-Hour Virtual Training: Lean Leadership, Quality and the Customer
Category: Drugs and Chemicals (Pharma) , Medical Devices , All FDA Regulated Industry , Hitech, Aerospace and Manufacturing , Quality Management , Quality and Safety , QMS, ISO 13485, CAPA , Supply Chain and Manufacturing , 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 , Life Sciences , QA/QC

3-Hour Virtual Training: Lean and the Manufacturing Process
Category: All FDA Regulated Industry , Quality and Safety , Food & Dietary Supplements , Drugs Regulations , Biotech Regulations , Life sciences QA/QC , Regulations & Guidances , Best Practices & GXPs , Life Sciences , Regulatory Affairs , Common FDA Regulations , QA/QC

GMPs for Medical Marijuana Production Operations
Category: Drugs and Chemicals (Pharma)

FDA Establishment Inspections - What to Expect?
Category: All FDA Regulated Industry

6-HR Virtual Seminar - SOP's and Work Instructions, Training, and Compliance in the Life Sciences
Category: All FDA Regulated Industry

FDA Regulatory Inspection and Audit Training: Pack of 6 Training Courses
Category: All FDA Regulated Industry