What is a Recorded Webinar?

Previously held webinars are available as recorded sessions, which you can view at your convenience. Registration orders are processed within two business days, after which participants will receive an e-mail confirmation with a link to the Recorded Webinar. After receiving the link to the Recorded Webinar, you have 15 days to view it.

What are CPIP^SM Recorded Webinars?

CPIP^SM Recorded Webinars are a group of Recorded Webinarswas developed to help individuals in preparation for the Certified Pharmaceutical Industry Professional^SM (CPIP^SM) examination..

The Certified Pharmaceutical Industry Professional^SM (CPIP^SM) credential recognizes “change agents” as the necessary ingredient to foster industry innovation and enhance drug product quality. The credential establishes a global competency standard for industry professionals, and candidates are assessed through demonstrated education, experience, and a rigorous examination. Completion of any of these seminars does not guarantee successful completion of the CPIP certification exam, and these seminars do not include every subject to the depth of what will be covered on the CPIP exam.

 See all available Recorded Webinars
 Technical Requirements and FAQs

New! Recorded Webinars

• Good Training Practices! Improving Compliance and Performance with Effective Training
• Overcoming Regulatory and Logistical Hurdles When Conducting Clinical Trials in India
• Enabling On-Demand: A Practical Alternative to the Traditional Method of Packaging and Labeling of Clinical Supplies

New! Complimentary Recorded Webinars

• Introduction and Update on ISPE’s New Risk-MaPP Baseline® Guide

Recorded Webinars for CPIP^SM Preparation

• This group of Recorded Webinarswas developed to help individuals in preparation for the Certified Pharmaceutical Industry Professional^SM (CPIP^SM) examination.
  
  
  CPIP^SM Webinars

Available Recorded Webinars:

• Airflow Pattern Visualization
• Basic Containment Terminology and Techniques
• Benchmarking Pharmaceutical Engineering and Management Costs
• Biopharmaceutical Inspections - The FDA Approach
• Blinded by Science - Functional and Unique Approaches to Blinding Clinical Trial Materials
• Clinical Trials: A Primer
• Deploying RFID in Pharmaceutical Manufacturing and Supply Chain Operations
• Distribution of Clinical Supplies to Emerging Economies
• Enabling On-Demand: A Practical Alternative to the Traditional Method of Packaging and Labeling of Clinical Supplies
• Equipping SMEs to Perform Effective Training
• European Clinical Trial Directive - An Update on Practical Aspects
• FDA Discusses Regulatory Aspects of the Biopharmaceutical Baseline Guide
• GAMP® Good Practice Guide: Validation of Laboratory Computerized Systems
• GMPs for the Contractor
• Going Modular - A Paradigm Shift in Pharmaceutical Facility Design and Delivery
• Good Training Practices! Improving Compliance and Performance with Effective Training
• Implementing Off-The-Shelf CTM Systems: Avoiding the Pitfalls
• Labs of the Future
• Leveraging Commissioning to Support a Risk-Based Approach to Qualification
• Managing Offshore Outsourced Software Development
• Manufacturing of Potent Drugs - An Industry Perspective on Facility Design, Measurements and Controls, as Presented to the FDA
• Metrics for Clinical Supplies Operations
• Overcoming Regulatory and Logistical Hurdles When Conducting Clinical Trials in India
• Pfizer Case Study - Using a Balanced Scorecard to Drive Continuous Improvement
• Presented by the FDA - The Quality Systems Approach to Pharmaceutical cGMP Regulations
• Proposed Revision to FDA Guideline on the Preparation of Investigational Products (Human and Animal)
• Risk Management in a Regulatory Context: Overview and Examples
• Stability Evaluation and Retest Dating of Clinical Trial Materials (Investigational Medicinal Products)
• Sterile Drug Products by Aseptic Processing: The New FDA Guidance
• South of the Border: Clinical Supply Challenges in South America
• The GAMP® Risk-Based Approach to Electronic Records and Signatures
• Top Five Critical Issues Facing the PAT Professional