Kristin Ding, Author at Verista

5 Reasons to Staff Qualified Trainers in a GMP Training Program

By Natasha Koolmees, Verista Quality Consultant When working in a Good Manufacturing Practices (GMP) environment, every process is standardized, yet…

May 2, 2023

Verista to Speak at ISPE Delaware Valley Chapter Symposium on Pharma 4.0

Verista, a leading business and technology company that provides systems, compliance, validation and quality solutions to life sciences clients, will…

May 2, 2023

Verista BioBytes – A Day in the Life of a Senior Validation Engineer

Verista Talent Acquisition Manager Alaa Eid interviews Verista Senior Validation Engineer Joel Mowatt to get deep focus on what it’s…

Apr 5, 2023

Training in Life Sciences: Is It Working?

By Natasha Koolmees, Verista Quality Consultant Quite often in the life sciences we get lost in the data but that…

Mar 29, 2023

The Missing Piece of Effective Change Management: Developing the Right Resources and Structure

In all regulated industries, an essential element of change management is documenting process changes in order to prevent unintended consequences…

Mar 22, 2023

Verista SVP, Mike Zanette, Featured in Article in BioFutures Magazine

BioFutures Magazine, a publication of the Indianapolis Business Journal, recently Interviewed Mike Zanette, Senior Vice President of Delivery Operations for…

Mar 20, 2023

Computer System Validation (CSV) in Life Sciences Part 1: Introduction to CSV

Introduction Pharmaceutical companies use computer systems for various purposes, including research and development, clinical trials, manufacturing, and distribution. To ensure…

Mar 7, 2023

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