Global BioPharmaceutical Resources Inc.

Brochure

Brochure

Forms

Registration Form

Hotel Information

Hyatt Regency New Brunswick

Limited rooms are available at the group rate until August 30th. To make resevartion go to link below or contact the hotel.

https://resweb.passkey.com/Resweb.do?mode=welcome_ei_new&eventID=2614992

Phone: 800.233.1234
Code: Global BioPharmaceutical Resources
Group Rate: $145 

Registration Fee

Before September 1: $695
After September 1: $995

Description

Single-Use Disposable Bioprocessing products have gained rapid acceptance by biopharmaceutical manufacturer worldwide. Single-Use Disposable products have reduced contamination rates, enhanced production throughput and decreased overall operating costs. Recent collaborations between leading filtration, container /closure, mixing and cell culture companies have resulted in fully integrated Single-Use Disposable Bioprocessing platforms and systems.
This seminar presentation examines the many facets of disposable bioprocessing systems that incorporate a wide scope of polymeric single-use products and will cover: Single-Use disposable Technologies, from upstream to downstream processes, are reviewed as related to the use of polymeric devices; how to increase productivity, reduce or eliminate cleaning and sanitization processes, reduce batch and cross batch contamination; and compare the significant material cost savings and reduction in operational expenses using disposables versus hardware. Specific attention will be given to the related applications used in the production of Biopharmaceuticals and pharmaceuticals.

Who Should Attend

Process Development Engineers and Scientists, Pilot-Plant Operations, Production Management and operation staff

Prerequisites

It is designed for the experienced as well as those new to biopharmaceutical processes.

Learning Objectives

Upon completion of this course, you will be able to:
• Identify applications where the use of disposables would be of practical advantage over hardware, e.g., cleaning validation
• Explain the concepts of disposable technology to assist in writing change control documentation
• Distinguish changes under the new regulatory process improvement guidelines, minor, moderate and significant
• Designate which processes and production areas would most benefit from a change to disposable products
• Describe the multiple cost saving analysis and plans for implementing and justifying the use of Single -Use Disposable Technology

Presenter

Mark A. Trotter, MSc., MBA
Trotter Biotech Solutions

About Presenter

Mr. Trotter, Owner and Business Consultant Trotter Biotech Solutions a consulting and training organization, supports the on-going technology transfer and training programs in the pharma, biologics, & biotech Markets. He completed graduate studies at Long Island University, NY, earning his MS in Medical Microbiology and earned his MBA in Finance. He has specialized training and work experiences in membrane technologies, including sterilizing, prefiltration, chromatography and single-use disposables technologies. Upstream fermentation to downstream applications such as separations, clarification and purifications processes, are areas of his subject matter expertise. Mr. Trotter has regulatory acumen that supports his expertise in process validations. process equipment manufacturers. Mr. Trotter has published numerous technical articles, book chapters and contributed expert editorial comment on these subjects. He is a member of PDA, Parenteral Drug Association.