This article also appears on MasterControl’s GxP Lifeline Computer system validation (CSV) can be a painful topic. That’s understandable, considering how much work goes into traditional CSV. Months of time are dedicated to the process, which produces piles of documentation. For companies working in industries regulated by the U.S. Food and Drug Administration (FDA), the […]
EDITOR’S NOTE: The following article is a Q&A with data integrity expert Matt Brawner from Sequence Inc.
To our Clients and Friends, Sequence is still open! We are diligently supporting our existing clients and looking to help others in a manner that is safe and restricts the spread of COVID-19. The COVID-19 (Coronavirus) outbreak continues to evolve in the US and around the world. To assure the safety of our families, friends, […]
Welcome to the Team, Joe! Sequence, Inc., is pleased to announce that Joe Barry has joined the firm as Director of Business Development for the New England region. Joe will be focusing on expansion, strengthening client relationships and insuring Sequence is positioned operationally to continue to provide services at the level of excellence Sequence is known for. Joe is […]
Continued Process Verification: Achieving Compliance and a Competitive Advantage, Upcoming Webinar Hosted by Xtalks Continued Process Verification (CPV) is a compliance requirement of all drug manufacturers. It presents formidable challenges unlike any other regulation, however, it also presents an opportunity to not only deliver compliance but also to improve organizational efficiency. In this free webinar, […]
Data Integrity: Trends, Pitfalls, Solutions, and Why DI Is Still Making Headlines by Matt Brawner Many working within the life sciences industry might describe themselves as more than familiar with the term data integrity . Companies have had years to properly ensure that their critical GxP data is complete, consistent, and accurate. So, why does […]