Medical Device and Diagnostics Industry Trends-Terri Sampo-04/22/2014 - 8:30am

Event Information
Event Topic: 
Medical Device and Diagnostics Industry Trends
Event Date: 
04/22/2014 - 8:30am
Event Location: 
Sunnyvale City Council Chambers, 456 West Olive Ave., Sunnyvale, CA
Speaker Information
Event Speaker: 
Terri Sampo
Event Speaker Title: 
Founder and Principal Consultant
Event Speaker Company: 
Clinical Trial Data Services
Event Speaker Bio: 

Terri founded CTDS in 2005 because she realized there was an unmet need in the marketplace for clients seeking a more efficient and cost-effective way to conduct clinical research. Since then, she has been responsible for directing all aspects of the data management and statistical services conducted at CTDS.

Terri is clinical data expert with over 15 years of experience designing, executing and analyzing clinical trials for various medical device, pharmaceutical and biotechnology clients. Over her career, she has contributed to many successful PMAs, 510 (k)’s and NDA with many new products being approved for use by the FDA and EU. Her specialties and interests are understanding the science behind each clinical trial, establishing client relationships and using a personalized approach to assist clients with obtaining product approval.

Prior to founding the company, Terri was a Project Manager/Biostatistician at Boston Scientific Corporation, a Senior Clinical Data Analyst for PLC Medical Systems and a bench scientist for Procept, Inc.

Terri earned her Master’s in Public Health (MPH) with a concentration in biostatistics and epidemiology at Boston University and a BA in Biology from St. Anselm College. She is a member of Society for Clinical Data Management (SCDM) and the Association of Clinical Research Professionals (ACRP).

Event Details
Event Details: 

The medical device industry has undergone significant growth over the last few years, while clinical and regulatory requirements have evolved to reflect an increasing level of sophistication. Terri will discuss the clinical and regulatory challenges unique to device and diagnostics trials and the impact of industry trends on trial design and execution.

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