Regulatory Focus™ > News Articles > 2019 > 9 > Three Ways to Save Time and Execute a Successful RIM Implementation

Three Ways to Save Time and Execute a Successful RIM Implementation

Posted 04 September 2019 | By Veeva Systems 

With an increasing amount of pressure to get new drugs to market faster, biotech and pharmaceutical companies are under a constant time crunch to perform. This is true in every stage of the regulatory process, including the implementation of a new RIM system, which if not done strategically can worsen the inefficiencies that it was designed to improve.

Watch this on-demand webinar to hear from two of Veeva’s subject matter experts, Lalana Dararutana and Serena Peirson, on ways to achieve a successful RIM implementation. Lalana brings extensive knowledge in regulatory affairs and regulatory operations including the implementation of Vault RIM, while Serena offers deep experience in clinical research spanning study conduct, data management/bio statistics, and system implementations across the R&D landscape. Together they’ll share three best practices to help you save time, improve system adoption, and keep your project on track from kick-off through post-deployment.


This article is sponsored and does not reflect the views or opinions of RAPS.

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