Advyzom
Theresa Dalla Riva has over 27 years of experience in regulatory submissions and operations within the pharmaceutical industry. Since April 2014, Theresa has served as the Head of Regulatory Submissions at Advyzom. Prior to this role, Theresa worked at Daiichi Sankyo from January 2012 to March 2014, initially as a Manager and later as a Supervisor in Regulatory Operations. Theresa's career also includes a significant tenure at Roche Pharmaceuticals from February 1996 to January 2012, where roles included eCTD Regulatory Submissions Publisher and Regulatory Sr. Publishing Specialist. Throughout these positions, Theresa has been responsible for ensuring the compliance and timely submission of regulatory documents to health authorities, as well as collaborating closely with various regulatory team members.
Advyzom
Advyzom is a leading boutique consulting company specializing in highly strategic regulatory and development advice and services for our partners in the pharmaceutical and healthcare industry. We are recognized leaders who insightfully seek and create opportunities throughout the product lifecycle to ensure it is successfully transformed for the client into a valuable therapy for patients. Our experienced team has successfully navigated across therapeutic areas, interacting with FDA Divisions and building global development programs. We collaboratively work within embedded or virtual solutions for clients by integrating into product teams, advising senior management and mentoring staff.