The Impact of Diabetes on the Workplace
With employees spending 40+ hours per week at their place of work, employers are uniquely positioned to help their employees manage prediabetes or type 2 diabetes. After all, this kind …
The New Behavior Change Model: How provider dynamics, health education and mobile technology have evolved to create a path to sustainable and scalable behavior change
Did you know that people only retain about 20% of what is conveyed in their doctor’s office? When it comes to health engagement and behavior change, John Moore, MD, Fitbit …
Top 5 Clinical Trends in Pharma and Biologics in 2018
Patricia Santos-Serrao, RAC, MasterControl’s director of clinical and regulatory solutions for pharmaceutical, blood, and biologics, discusses the five clinical trends that currently having the biggest impact on the pharmaceutical and …
The Evolution of Medical Device Clinical Trials: Their Background and a Look Toward the Future
Global regulatory affairs and compliance expert David Dills provides a comprehensive overview of the evolution of medical device clinical trials regulations and explains how in-depth knowledge of regulatory requirements and …
5 Ways Walking Can Help You Better Manage Diabetes: Ways to help get type 2 diabetes under control
Over a hundred million people in the U.S. are living with type 2 diabetes or prediabetes.(1) In fact, 90% of people with prediabetes don’t even know they have it.(2) But here’s the …
How Global Pharmaceutical Leader Lundbeck Boosted Security and Efficiency through Cloud Security.
“We liked that Umbrella’s intelligent proxy would give us granular protection without the performance impact of a traditional web proxy.” – Torben Olsen, Corporate Information Security Manager, Lundbeck
ZZZs and $$$s: How sleep impacts the bottom line
Nearly one in three adults report one or more symptoms of insomnia —and these fatigue-related productivity losses have been estimated to cost $2,280 per employee annually in the U.S. That’s …
Eliminate TMF Inadequacies in Your Clinical Trials
To comply with regulatory requirements pertinent to clinical trials, every organization engaged in a clinical trial must manage and maintain all trial-related content, documents, and data in a manner that …
Top 8 Obstacles in Pharma & Biologics Product Registration & Submission Management
For pharmaceutical and biologics companies, the path to a global product launch is full of obstacles that could result in delays to registrations, many of which can be avoided with …
How to Address 10 Common Pains in Dossier Management & Product Registration
While the process for obtaining a device clearance or premarket approval (PMA) in the United States is not the same as applying for a Shonin in Japan or a CE …
