With the COVID-19 pandemic disrupting global supply chains and forcing many to work from home, life sciences organizations are under pressure to quickly adapt while adhering to rigorous compliance standards.

Please join experts from Thermo Fisher Scientific, Becton Dickinson and DocuSign, as they discuss best practices on the following:

Digital transformation beyond organizational silos

Accelerate regulatory and quality processes to adhere to GxP guidelines and global standards such as GDPR and eIDAS

Quickly stand-up and validate a technology within weeks to adhere to the FDA’s 21 CFR Part 11 requirements

The challenges and opportunities COVID-19 poses on the life sciences industry

Implement a technology across your organization and at scale 

Featured Speakers

Dewey Phan

Associate Director, Corporate Quality
Becton Dickinson

Dewey Phan is currently an Associate Quality Director at Becton Dickinson. His main responsibility is to harmonize different processes in the quality management system including software validation, Part 11, laboratory controls, and product cybersecurity.  He is also the business owner for several quality IT systems including Part 11 DocuSign. Prior to BD, Dewey worked in the R&D and Quality functions at the blood banking diagnostic division of J&J. Dewey has a BS in Biomedical Engineering from Boston University and an MBA from Rutgers University.

Gord Keith

Technical Operations Manager for Packaging Engineering and Technical Documentation, Pharma Services Division
Thermo Fisher

Gord Keith has over 20 years’ experience in the Pharma industry. In his current role, he’s the Technical Operations Manager for Packaging Engineering and Technical Documentation for Thermo Fisher Scientific’s Pharma Services Division. Gord has played an integral role in DocuSign Part 11 module rollout and adoption at Thermo Fisher. His site went live with DocuSign in March 2019 with three main use cases and a pool of 35 users. Since then, they continually worked to expand their use of the system and now have over 15 use cases and more than 700 users on the system. 

Carolina Rivera

Sr. Product Manager

Carolina Rivera is currently a Sr. Product Manager at DocuSign. Since she joined DocuSign, her primary focus has been growing DocuSign’s Healthcare and Life Sciences vertical, continually innovating on the products and strategy for this sector. Carolina has over 9 years’ experience working in the business software space. Prior to DocuSign, she worked at Deloitte Digital, leading digital transformation projects across varied industries. She also worked as a product manager for a supply chain SaaS company, Elementum, helping organizations simplify global operations using predictive analytics. Carolina has a BS in Industrial and Systems Engineering from Texas A&M University and an MBA from Stanford University.


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