Kristin Ding, Author at Verista

Webinar: AmplifyBio Achieves Compliance and Advances Their Digital Strategy Using Pharma 4.0

This webinar covers how Verista assisted AmplifyBio, a preclinical CRO, in their journey to go paperless by incorporating industry best…

Jun 1, 2023

Are You Ready for Pharma 4.0, Digital Maturity and Digital Transformation?

Pharma 4.0 is all about bringing a new era of digital transformation and automation, powered by innovative, advanced technologies, into…

May 30, 2023

CQV Part 3: Overcoming Challenges in the Pharmaceutical, Biotech and Medical Device Industries

Commissioning, Qualification, and Validation (CQV) are critical steps in the pharmaceutical, biotech, and medical device industry to ensure the quality…

May 17, 2023

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

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