DistillerSR Best Practices Session

Join us on May 16 at 11 am EDT for a special session to learn more about how Enterprise Evidence Management can help you and your teams improve collaboration, reduce operational costs through a consistent approach for data collection, curation, and analysis.

Agenda – May 16 at 11am EDT

 

Introduction

Madhu Vijayakumar, Product Marketing Manager at DistillerSR

 

Enterprise Evidence Management Best Practices

Dr. Sara Paquette, PhD, Clinical Consultant and Expert in Medical Writing and Clinical Claims Management

 

DistillerSR Demo

Madhu Vijayakumar, Product Marketing Manager at DistillerSR

 

Q&A

  • Madhu Vijayakumar, Product Marketing Manager at DistillerSR
  • Dr. Sara Paquette, PhD, Clinical Consultant and Expert in Medical Writing and Clinical Claims Management

Key Learning Objectives

  • Consolidate all evidence into a single, centralized location for easy access and streamlined management.
  • Implement access controls to regulate data access, fostering collaboration while safeguarding sensitive information.
  • Develop a company-wide strategy to encourage the reuse of existing data, minimizing duplication of effort and enhancing efficiency.
  • Establish uniform procedures for evidence collection and review to ensure consistency and accuracy throughout the process.
  • Evaluate and refine evidence management practices to adapt to changing needs and optimize effectiveness.

Register for the Session

“We just started testing out CuratorCR, and we believe upwards of 50% of the literature review work will already be completed when we move from one legacy device to another — the device application and the outcomes to be monitored will be distinct, but the reference data pool will largely be the same. Mentally speaking, it will be a game changer to start a new literature review knowing a significant portion of the work has already been completed,”

Shelley Jambresic, Senior Clinical Evaluation Manager at Geistlich Pharma AG