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.

Join this 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.

Featured Speakers

Serena Peirson

Practice Manager, SMB
Veeva

Serena Peirson brings over 20 years of experience spanning many areas across Life Sciences. She began her career as a CRA and Clinical Project Manager then expanded to providing software solutions to support CTMS, eSubmissions, Risk-Based Monitoring, and other cloud products. Serena continues to guide innovation with new technologies serving many different functional areas such as Biostatistics, Cloud Adoption, Metrics & Reporting, Product Management, and Operational Excellence.

Lalana Dararutana

Practice Manager, Vault RIM
Veeva

With 18+ years of expertise in Regulatory Affairs and Regulatory Operations, Lalana is well-versed in global regulatory requirements, compliance considerations and processes for submission management. She has led operational change management initiatives, business analysis projects, process modeling efforts and implementations of content management systems for life sciences. Lalana is an active contributing member of special interest and standards organizations such as the EDM Reference Model working group and IRISS, maintaining a keen understanding of current challenges faced by life sciences companies as well as emerging technology solutions.

Rachel Belani

Director, Vault RIM
Veeva

Rachel Belani has 15 years of experience in the pharmaceutical industry.  She is currently a member of the global regulatory strategy team at Veeva. Before joining Veeva, Belani’s career was focused on developing solutions and processes for life sciences organizations, with a specific focus on regulatory, clinical and safety.  She started off her career at Actelion Pharmaceuticals where she served as the Americas lead for R&D systems and processes, including ECM/EDMS, archiving, CTMS, LMS, ERP, analytics and reporting for clinical development.  Following Actelion, Belani transitioned into a consulting role where she helped life science companies define and optimize their business and solution architecture, from both a clinical and regulatory perspective.

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