Monitoring represents a significant portion of clinical trial costs. Join this webinar to learn how companies are challenging traditional processes and taking a new approach to monitoring activities to improve efficiency.

Speakers Drew Garty and Henry Galio from Veeva will share how to:

  • Streamline monitoring trip reports and view enrollment metrics in real-time

  • Optimize your execution of targeted SDV

  • Use operational data to improve study design

  • Simplify ancillary reviews and assessments of clinical data

  • Improve coordination across sites, CRAs, and data managers

They will also show how connecting EDC and CTMS data can eliminate manual processes and improve efficiency across the entire monitoring lifecycle.

This New Year, learn how to take a fresh look at your own monitoring processes to save time and money.

Featured Speakers

Drew Garty

Chief Technology Officer, Vault CDMS
Veeva Systems

As Chief Technology Officer, Vault CDMS, Drew shares and collaborates with customers, partners, and the industry to set vision and direction of Veeva’s CDMS product. Drew’s career in pharmaceutical technology spans over 20 years and includes significant experience in eClinical system architecture, design, and development, as well as process design, solution validation, and international implementation and support.

Henry Galio

Senior Director, Vault CTMS
Veeva Systems

Henry Galio is responsible for the overall market strategy and direction of the Veeva Vault CTMS application. With over 30 years of experience in life sciences and 18 years in developing and implementing clinical trial systems and clinical data analytics, Henry is an expert in clinical operations software, business process optimization, and CTMS efficiency. 

Date:  Thursday, January 30, 2020
Time:  11am ET / 8am PT
Duration:  1 Hour

Register now for this webinar