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San Diego Convention Center

Jun 16, 2024 7:00 AM - Jun 20, 2024 3:00 PM

111 W Harbor Drive, , San Diego, CA 92101 , USA

DIA 2024 Global Annual Meeting

Join us at the premier life sciences conference, celebrating our 60th anniversary! Discover 180+ sessions on Cell and Gene Therapy, Decentralized Clinical Trials, AI, ICH, and more. Get ready to tackle challenges, improve skills, network, and drive change for healthcare at DIA2024.

International Harmonization to Support Pharmaceutical Quality and Lifecycle Management

Session Chair(s)

Amanda Marie Roache, MS

Amanda Marie Roache, MS

Senior Director, Science and Regulatory Advocacy

Phrma, United States

Since establishment in 1990, the International Council for Harmonisation (ICH) has expanded its global footprint to harmonize requirements for the development of medicines and to increase patient access to medicines. Importantly, ICH’s quality portfolio serves to support continual improvement and innovation in biopharmaceutical manufacturing. In 2018, ICH published its quality mission to “develop a harmonised pharmaceutical quality system applicable across the lifecycle of the product emphasizing an integrated approach to quality risk management and science” driving the development of several new guidelines addressing topics on lifecycle management, quality risk management, continuous manufacturing, and analytical procedure development and validation. With ICH’s expansion, it has prioritized the adequate implementation and adherence of guidelines through its work to promote training and periodically conduct a survey to assess guideline implementation by ICH Members and Observers. This session will provide global regulatory and industry perspective regarding progress made on the ICH quality mission and explore future opportunities to achieve greater harmonization and encourage the global community to embrace the science and risk-based approaches. Case studies will be presented highlighting the objectives and work to facilitate a globally aligned approach to implementation of ICH guidelines.

Learning Objective : Describe objectives of international harmonization through ICH to promote innovation and facilitate more efficient lifecycle and post-approval change management; Discuss status of key ICH Guidelines such as Q13, Q12 and Q14 and their implementation globally; Evaluate case studies and identify opportunities to advance global harmonization.

Speaker(s)

Connie  Langer, MSc

Lifecycle Strategies at the Interface Between ICH Q12 and ICH Q14

Connie Langer, MSc

Pfizer Inc, United States

Senior Director

Nina S. Cauchon, PhD

ICH Q14: Analytical Procedure Development and Lifecycle Management

Nina S. Cauchon, PhD

Amgen, United States

Director Regulatory Affairs CMC

Sau L Lee, PhD

FDA Update

Sau L Lee, PhD

FDA, United States

Deputy Super Office Director, OPQ, CDER

Satomi  Yagi

Update from Japan on Q12

Satomi Yagi

Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Reviewer, Office of New Drug III

Anabela  Marcal, PharmD

Update from EMA

Anabela Marcal, PharmD

European Medicines Agency, Netherlands

EMA Liaison Official to the US FDA

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