Expediting Timelines without Sacrificing Quality

Expediting Timelines without Sacrificing Quality
August 6, 2019 YPrime

In a poll conducted at a YPrime Expert Community event, attendees responded that 24 weeks or more prior to first site ready was an ideal timeline for implementing eCOA. However, the scope of work tends to expand starting at the kickoff meeting while the timeline remains the same. In this webinar, the panelists, led by Donna Mongiello, discuss how to adapt to the larger scope within the original timeline without sacrificing quality.

Watch the video to find out more about expediting eCOA timelines.

VIDEO

Expediting Timelines without Sacrificing Quality

RELATED CONTENT

Getting Better Together Initiative eCOA Lexicon

Getting Better Together Initiative eCOA Lexicon

How to Get the Most Out of Your eCOA Data

How to Get the Most Out of Your eCOA Data

Is BYOD right for your  eCOA Clinical Trial?

Is BYOD right for your eCOA Clinical Trial?

LATEST CONTENT

Effective Use of IRT in Decentralized and Hybrid Clinical Trials

Effective Use of IRT in Decentralized and Hybrid Clinical Trials

Improving DCT Technologies for Efficient and Personalized Delivery

Improving DCT Technologies for Efficient and Personalized Delivery

The Importance of IRT in the Decentralized Clinical Trial Landscape

The Importance of IRT in the Decentralized Clinical Trial Landscape