ACT

JAN. 12/2016

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news roundup

Nimblify Participant Payment System Debuts

Participant Payments provides clinical research sites the choice to pay participants via reloadable debit card, direct deposit or check, without additional work for the site.


New Clinical Trial Registration Service Launches

EveryClinicalTrials is comprised of two primary services, Protocol+ for the registration of trials and Results Services for the publications of trial results.

ACRES, ActivMed Focus on Site Accreditation

ActivMed will collaborate with ACRES in developing standards and processes for ACRES site accreditation and professional development programs for research staff.

In this edition

Nimblify Participant Payment System Debuts
A Guide to Risk-Based Study Start-Up
Califf Discusses Diversity and Data
Risk-Based Monitoring Update-- Case Study Examines Two RBM Frameworks

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articles

A Guide to Risk-Based Study Start-Up

This article examines how big data can be used to overcome cumbersome study-start up processes.


6 Ways Clinical Supply Can Protect Blinding in Trials

Challenges including electronic risk and adaptive designs, introduce the possibility of releasing sensitive, unblinded, information to trial personnel.

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Blog Posts

Califf Discusses Diversity and Data

Califf described the many challenges to finding a balance between clinical trials large enough to assess all relevant populations and small enough to include deep data on each patient.


Adaptive Pathways: Pilot or Plot?

The EMA is being accused of colluding in a conspiracy to favor drug firms at the expense of patient protection.


Risk-Based Monitoring Update

Case Study Examines Two RBM Frameworks


Excel-Based (RACTs) Go to the Cloud


Infinity Pharma Uses Medidata RBM in Phase III Trials


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Lisa Henderson
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