Kristin Ding, Author at Verista

CQV Part 2: Common Challenges in the Pharmaceutical, Biotech and Medical Device Industries

Commissioning, Qualification, and Validation (CQV) is a crucial process in the pharmaceutical industry to ensure that equipment, facilities, and processes…

May 17, 2023

CQV Part 1: A Critical Element in the Pharmaceutical, Biotech and Medical Device Industries

Commissioning, Qualification, and Validation (CQV) is a crucial process in the pharmaceutical industry that ensures that facilities, equipment, and processes…

May 10, 2023

Verista BioBytes – Discussing CQV and Overcoming Changing Regulations in the Life Sciences

Verista Senior Delivery Manager Juli Hood discusses Commissioning, Qualification & Validation (CQV) in conjunction with adapting to the changing compliance…

May 8, 2023

Computer System Validation (CSV) Challenges in Life Sciences (Part 2)

As discussed in Part 1 of this blog series, pharmaceutical, biotech and medical device companies use computerized systems for various…

May 4, 2023

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

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