In this ISSUE

Regulatory Approval in India: An Updated Review

CTMS: What You Should Know

Real-World Evidence Studies

Real-World Data

Utilizing Real-World Data Captured During Commercial Programs

In part three of his blog series, Tim Davis takes a look at how electronic platforms can support RWD data capture in commercial pharma programs.
... /Read more/

Exclusive Interviews from the 2017 DIA Global Annual Meeting
Check out these exclusive interviews from the 2017 DIA Global Annual Meeting in Chicago, IL, conducted by the editors of Pharmaceutical Executive and Applied Clinical Trials. Whether or not you attended the event, here is your chance to gather insights from featured industry professionals.

Watch Videos

Clinical Operations

Methods for Clinical Trial Issues Identification and Resolution

Moe Alsumidaie outlines the process of identifying, diagnosing, correcting, and resolving issues in a quality management system QMS) issues management repository.
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Tomorrow's Clinical Trial, Powered by Modern EDC
See how to cut study build time in half, eliminate migrations, and remove the need for source data verification (SDV).

See a preview and watch the full webinar here.

Calendar

/ eCOA/ePRO 2017 12/13-12/14 /

/ Clinical Data Disclosure and Transparency 1/30-1/31 /

/ Clinical Trial Budgeting & Forecasting 2/22 /

Engaging Rare Disease Patients & Accelerating Clinical Development
In a series of white papers, PRA experts discuss the barriers drug developers face when positioning a new trial in the rare disease space and how to minimize these while engaging with the right patients.

Download the White Papers

Three-Step Approach

Three Steps to a Successful Combination Product Trial

Sponsors can streamline the design and execution of their clinical trials for combination drugs by following this three-step approach.
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The Clinical Trial of the Future is Here - Now: Understand how technology is transforming clinical development - now and in the future
Live Webcast: Wednesday, December 13 at 11:00am EST

Analytic Software

Beyond RBM: How Intelligent Analytics can Drive Value and Support ICH Compliance

Steve Young explores the benefits that organizations can reap by effectively applying the core principles included in the ICH E6 update—and the significant opportunities from intelligent analytics and centralized statistical monitoring.
... /Read more/

Beyond #Buzzwords: How to deploy wearables and remote devices to transform your clinical trial execution
On Demand

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eClinical

Machine Learning Within the Clinical Trial Process

Machine learning technology is finding its way into today's clinical trials, as developers look for ways to leverage more qualified data to help diminish patient risk and enhance quality, writes Adam Ross Miller.
... /Read more/

The Benefits of a Data-driven Approach to Feasibility
Live Webcast: Tuesday, March 20 at 11:00am EDT

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Lisa Henderson
Editor in Chief
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Todd Baker
Group Publisher
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