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18-19 November 2019
Radisson Blu Edwardian Grafton,

Continuous Manufacturing for Biopharmaceuticals

On this 2-day course you will discover how to develop a continuous bioprocess, and compare the pros and cons with batch manufacture

Course Overview

How easy is it to integrate continuous processing into manufacturing your biological drug, and what are the benefits and disadvantages?

Over the course of two days you will build on your understanding of how to effectively develop a continuous process and navigate the regulatory framework associated with it. Using interactive exercises and case studies to consolidate your knowledge, you will evaluate whether adopting a continuous process is the right decision for your manufacturing department.

What will you learn?

The pros and cons

Learn important definitions and advantages and disadvantages to continuous manufacturing, including increased efficiency and real-time analytics

How to adopt a continuous process

Understand how to develop a continuous process, including upstream and downstream aspects

Regulatory requirements

Familiarise yourself with the regulatory landscape and important ICH guidelines

The tools of the trade

Learn what equipment is needed for continuous manufacture and the importance of cleaning specifications in continuous processing

The differences from batch manufacturing

Understand the importance of quality assurance and process validation for continuous production, as well as consider key differences with batch manufacture

Who is this course for?

This course should be attended by anyone who works in biopharmaceutical manufacturing and is considering adopting a continuous process.

Relevant departments would include:

  • Management
  • Process validation
  • Processing Engineering
  • Quality Assurance
  • Regulatory Control
  • Manufacturing Management

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