Introduction: In this article, we will examine two key aspects of quality management: quality assurance and quality control. These are two broad approaches that businesses […]
It is often said that as we grow older, it becomes harder to learn new skills, especially language skills. Taking a second or third language […]
What is 21 CFR Part 11? 21 CFR Part 11 establishes US FDA regulations on Electronic Records & Electronic Signature (ERES) which includes electronic submissions […]
In this series, PDG’s Ann Stott, a 20+ year veteran of the Life Science industry, shares her perspective on how to become more strategic in […]
There’s no denying that changes in the world economy are having an effect on every industry. And the Life Sciences industry is feeling the effect […]
Is it difficult to get new behaviors from an experienced sales team? The tenured sales force responsible for Genzyme’s Multiple Sclerosis product (AUBAGIO®) had seen […]
Join PDG and Pfizer at the ATD International Conference When you work in the life sciences industry, change is a constant. And when you're one […]
For highly regulated medical device companies and life science industries, it has become a challenge to achieve 21 CFR Part 11 compliance and a matter […]
Laboratories in the field of life sciences play an essential role in research, testing, and product development for medical devices and drugs of all kinds. […]
A large portion of the success of the pharmaceutical industry revolves around successful sales. Without good sales reps, the industry could easily falter. But selling […]
The regulations from the US Food and Drug Administration (FDA) that apply to how various life sciences companies handle electronic files and electronic signatures is […]
Whether a biopharmaceutical company is large or small, research is essential to moving industry knowledge forward and achieving the company’s mission. Does biopharmaceutical research fall […]