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HomeResearch & DevelopmentBioprocess Facility Design – Layout Rules and Configurations

Bioprocess Facility Design – Layout Rules and Configurations

Teachers
Erich Bozenhardt
Herman Bozenhardt
Category:
On-Demand Courses/ Regulatory & Compliance/ Research & Development/
Clear
Duration: 90 minutes
On-Demand
Includes handouts
  • Description
  • Who Should Attend
  • What To Expect

Description

COURSE DESCRIPTION

OVERVIEW

Expansions and renovations to existing biological facilities – and construction of new facilities – provide a unique opportunity to rethink basic design strategies and use new technologies to build a better facility that will reduce costs and improve compliance. This webinar will discuss how process and regulations are changing the modern biotechnology facility and process design paradigm.

There are multiple variables that must be considered in the layout of a biopharmaceutical facility, and many of these variables are interdependent. The adoption of modern process systems and techniques are allowing for a shift in the balance of those variables to enable smaller and more flexible facilities. This will include the elimination of many of the utility areas, allow for rapid product/process change over, greater product integrity, and increased compliance. This webinar will explore modern facility design options and configurations, and the realities of building a facility around the today’s process technology.

LEARNING OBJECTIVES

Join us for this 90-minute, online seminar, where you will learn:

  1. What impact single use systems (SUS) will have on facility design
  2. Basic principles of facility layout
  3. Layout rules and options
  4. The three key basic layout models for all modern biotech design
  5. How to develop smaller flexible facilities that will allow your operations to scale without pain

Who Should Attend

WHO SHOULD ATTEND

This course will be of benefit to anyone involved in the production, engineering, or quality operations of biotech facility or a team member assigned to a new biotech project. Additionally, those for communicating internally with engineering or operations personnel responsible for new production will find this course extremely beneficial.

What To Expect

WHAT TO EXPECT

HOW TO PARTICIPATE

This webinar is offered on-demand. With your course purchase, you may view the previously recorded live session at your convenience (available for 30 days). Access to the on-demand webinar will be made available via email within 1 business day after your purchase. To access the course, you need only a computer with internet access and the log-in credentials.

THE TRAINING PLATFORM

Our webinar platform combines the convenience of online training with the live interactivity of the classroom. Quizzes, case studies, break-out sessions, and assessments are often incorporated into the training . Other ancillary materials can be downloaded from the “Handouts & Resources” area in the virtual classroom. Each course purchase includes a completion certificate issued to the participant after the course.

USER AGREEMENT

Your registration fee for a single participant entitles you to one telephone dial-in and one online course log-in per site. Course testing capabilities, stored results for training records, and completion certificates are available for only one registrant per single participant course purchase. For multiple participants, please purchase more than one registration or consider our 5 or 10 participant packages.

Is this course right for me? We’d be happy to help you select the right training course to meet your needs.
Give us a call at 215-675-1800 (9am – 5pm EST, M-F) for assistance.

About Instructors

Erich Bozenhardt
Erich Bozenhardt has 11 years of experience in the biotechnology and aseptic processing business and has led several biological manufacturing projects, including cell therapies, mammalian cell culture, and novel delivery systems.
Herman Bozenhardt
Herman Bozenhardt has 41 years of experience in pharmaceutical, biotechnology, and medical device manufacturing, engineering, and compliance.

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Clear
Duration: 90 minutes
On-Demand
Includes handouts

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Cleaning Validation Cleanroom Clinical Trials Cloud CMOs Computer Systems CRAs CROs Data Integrity Device eCTD EMA Equipment Facilities FDA GCP GDP GLP GMP HIPAA Human Error ICH Informed Consent Inspections Instructional Design Management manufacturing Marketing MDR microbial control Process Validation Project Management QMS Quality Quality by Design Quality Risk Management Remote Monitoring Risk Risk-Based Monitoring Root Cause Analysis Site Monitoring SOPs Training Trial Master File Upcoming Courses

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The Life Science Training Institute helps pharma, biotech, and medical device companies build knowledgeable, compliant workforces by providing training from drug discovery through commercialization. We are dedicated to advancing careers of those working to develop new therapies and to protect patient safety.

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