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Hyatt Regency Miami

2020 年 02 月 24 日 7:00 上午 - 2020 年 02 月 25 日 5:45 下午

400 S.E. Second Ave, Miami, FL 33131

Latin America Regulatory Conference

Session 4: Continuous Manufacturing and ICH Q13

Session Chair(s)

Maria  Guazzaroni Jacobs, PHD

Maria Guazzaroni Jacobs, PHD

Director, Quality Intelligence, Global Supply

Pfizer Inc, United States

Continuous manufacturing (CM) is used to manufacture, produce, or process materials without interruption. There are several advantages of CM, such as being an integrated processing with fewer steps, no manual handling, shorter processing times, and increased efficiency. They are more flexible operations that use smaller equipment and facilities. They allow for online monitoring and controls which result in increased and consistent product quality. During this session, an agency representative in the ICH Q13 team will give an update on the ICH guide on CM and an industry representative will discuss industry experience with CM and present case studies. The two presentations will be followed by a Q&A panel.

Learning Objective :

Upon completion of this session, the participant should be able to:

  • Understand the benefits and challenges of using continuous manufacturing
  • Learn how industry and regulators are working together under ICH Q13 to harmonize the approach to CM
  • Discuss with colleagues from both industry and regulatory agencies on lessons learned when applying CM

Speaker(s)

Maria  Guazzaroni Jacobs, PHD

Speaker

Maria Guazzaroni Jacobs, PHD

Pfizer Inc, United States

Director, Quality Intelligence, Global Supply

Manuel  Osorio, PHD

Speaker

Manuel Osorio, PHD

FDA, United States

Senior Scientist for Emerging Technologies

Daniel  Blackwood

Speaker

Daniel Blackwood

Pfizer Inc, United States

Director, Pharm Science Technology and Innovation

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