The aspirations in the industry are increasingly focused on ensuring that process, people and technology come together to accelerate the product submissions for market authorizations while reducing overhead on product lifecycle submissions management. Aspirations from organizations such as IFPMA will be discussed and approaches to elevate best practices leveraging latest technologies will be presented.
Learning Objectives:
Understand the goals in the industry for Convergence and Reliance that both IFPMA and ICMRA as well as ICH are supporting to drive efficiency the time to market and capacity of health authorities.
Understand opportunities that can be embraced to optimize the regulatory process. Understand approaches that technology could be applied to enable faster time to market.
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