Modular construction, whether via "facility" or "skid" modules, is becoming more popular as an enhancement to the project delivery method for new pharmaceutical manufacturing facilities. The approach offers advantages such as improved quality, increased flexibility, and faster completion and allows owner-operators to minimize site disruptions and speed validation. However, modular projects must be handled differently from traditional plant construction projects, and require a "paradigm shift" in both project planning and execution.

In this Recorded On-line Seminar, we will discuss some of the issues involved in designing and building new facilities using pre-built modules. Participants will receive an overview of the technical and logistical steps involved in utilizing and executing a modular facility project. We will discuss the advantages and challenges of the planning phases, resource allocation, changes and flexibility aspects of facility modularization, to better prepare those considering modularization for their next project.

Learning Objectives
At the end of this Recorded On-line Seminar, participants will be able to:

• Discuss how to go about considering modular technology properly in a project timeline 
• Identify issues of owner resources, clarity of functional requirements, and avoidance of redundancies
• Describe how schedule compression and parallel activities are compared to traditional construction along with change control and validation aspects
• Discuss issues of what can and cannot be done with modular technology along with lessons learned from previous modular projects

Who Should Attend

•  Professionals involved with new facility design and master planning
• Those involved in process engineering, project management, and senior management who are considering modular technology for a new project.

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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.

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