26-27 November 2020
Radisson Blu Edwardian Kenilworth,
Continuous Manufacturing for Biopharmaceuticals
Discover strategies to develop a high quality continuous bioprocess to improve manufacturing efficiency
Our number one priority is the safety of our delegates and colleagues, and there are always measures in place at our venues to safeguard your health and safety. There are extra measures in place for 2020 in light of developments with COVID-19.
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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
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:
- Process validation
- Processing Engineering
- Quality Assurance
- Regulatory Control
- Manufacturing Management