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International Harmonization to Support Pharmaceutical Quality and Lifecycle Management
Session Chair(s)
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)
Lifecycle Strategies at the Interface Between ICH Q12 and ICH Q14
Connie Langer, MSc
Pfizer Inc, United States
Senior Director
ICH Q14: Analytical Procedure Development and Lifecycle Management
Nina S. Cauchon, PhD
Amgen, United States
Director Regulatory Affairs CMC
FDA Update
Sau L Lee, PhD
FDA, United States
Deputy Super Office Director, OPQ, CDER
Update from Japan on Q12
Satomi Yagi
Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Reviewer, Office of New Drug III
Update from EMA
Anabela Marcal, PharmD
European Medicines Agency, Netherlands
EMA Liaison Official to the US FDA
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