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Discover how AI is revolutionizing pharmaceutical validation processes. Join industry experts to explore enhanced efficiency, compliance, and automation in regulated environments.

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Computer Software Assurance (CSA) is the FDA-recommended approach to speed up Computer System Validation (CSV) without increasing the risk —…

ALCOA has been the hallmark of data integrity best practice for years and it’s evolving. ALCOA++ represents data integrity for the new digital age and provides the information needed to ensure compliance and good document practice well into the future. In this webinar, Kneat’s data integrity expert Olivia Calder explores the challenges of ensuring data integrity and the new requirements as technology evolves.
Hosted by digital validation experts Pablo Munoz Pierattini, CSV & CSA Manager at CSV Life Science, and Paul Smith, Partner Success Manager at Kneat, this session includes digitalization best practices for validating automated technologies, Distributed Control Systems (DCS) and Supervisory Control and Data Acquisition (SCADA), ensuring organizations meet all regulatory requirements.

Contract manufacturers in life sciences, whether CDMO or CMO, face extensive validation challenges across the entire development and manufacturing lifecycle,…

Discover how Validation 4.0 is transforming life sciences with digital innovations that boost efficiency, compliance, & product quality. Join our webinar!

ALCOA++ and the Future of Data Integrity ALCOA has been the hallmark of data integrity best practice for years and…

AI is revolutionizing every industry across many functions, including validation. Learn how AI is impacting process validation in our webinar.

Utilizing Digitization for Risk-Based CSV As more digital systems emerge to help life sciences manufacturers enhance quality, the burden on…

Digital validation solutions like Kneat do more than make the lives of validation professionals easier. They deliver deep efficiencies with significant return on investment for your company. In this webinar, our experts walk you through how to calculate the ROI of digital validation, so you know what to expect, and how to get it approved by your management.

2024 State of Validation Insights and Trends Discover the latest insights and trends from the 2024 State of Validation report…

Mastering Pharma 4.0 Validation Challenges With Technology Validation is foundational for organizations prioritizing a Pharma 4.0 initiative as it touches…

Acing an Audit: What to Do Before, During, and After an Inspection In this webinar hosted by ISPE, Kneat Solutions’…

In this webinar, Kneat’s expert, Mo Brar, will explore electronic batch records and tools you can use to deploy them effectively at your company while mitigating the risks associated with implementing new technologies.
In this webinar, you’ll hear from industry expert Luca Zanotti Fragonara at PQE Group on the potential of AI for Pharma, regulatory considerations, and the use cases of AI in pharma that will drive future success.
Join Kneat Solutions and Kathianne Ross, a compliance expert from Fujirebio Diagnostics, to learn the essential ALCOA+ principles of data integrity, providing you with the foundation to fortify your compliance efforts and thrive in upcoming audits.

2024 Validation Trends: Unveiling Insights & Innovations The State of Validation is an annual report on practices, trends, and challenges…

Better Together: Kneat’s New Partner Program Solid, repeatable growth, deepened client relationships, and deeper product and service offerings. It’s all…

Harnessing Kneat Implementation as a Change Agent for Harmonization In today’s fast-paced and regulation-driven landscape, achieving harmonization across global operations…

Join us as we guide you through the intricacies of creating a robust Validation Master Plan (VMP) and Validation Plan (VP) and show you how our digital validation solution, Kneat Gx, amplifies the efficiency and effectiveness of your validation plans.

Leveraging Supplier Activities and Testing Under CSA To streamline CSV, the U.S. FDA has recommended a number of improvements to…

Process Validation 4.0: Overcoming Process Validation Challenges With Technology Process validation in the context of Pharma 4.0™ puts significant emphasis…

Every project relies on commissioning and qualification to get up and running. Faster C&Q means faster time to market — Is your C&Q program as efficient as it can be? In our upcoming webinar, we explore how digital validation streamlines C&Q to improve productivity, enhance compliance, and reduce costs.

Muda and Mura Mastery Enhancing Quality and Validation Through Digitalization and Process Optimization The pharmaceutical industry is transforming. As global…

The State of Validation 2023: Industry Report in Review Validation is always evolving and using the latest techniques and tools…

Futureproofing Your CSV Program The use of technology is expanding at an ever-increasing rate and for teams responsible for Computer…

True Copy Verification: Getting it Right True Copy verification is a required component of any paperless validation system, critical to…

Amplifying Your Kneat Gx Implementation With Integration Kneat Gx has a proven ability to accelerate production by reducing validation cycle…

Kneat Solutions and Agidens NV are excited to run Managing Your Equipment Lifecycle to Mitigate Risk and Drive Value. Hear…

How to Overcome Challenges With Software Verification & Validation Join our panel of industry experts from Kneat and global leader…

Process validation is the bedrock of good manufacturing practice, it’s also the first step to realizing significant time and cost savings in validation. Make sure you’re in position to succeed by watching our webinar, The Three Stages of Process Validation with our expert, Olivia Calder.
Join us for our latest webinar Using Digital Validation to Unlock CSA’s Benefits. You will learn how to shift from CSV to CSA through risk-based critical thinking, why a digital validation solution is the best way to realize CSA’s benefits, and much more!

Data Process Mapping: Effective Data Integrity Management Through Digitization Join us for a ‘Data Process Mapping: Effective Data Integrity Management…

Shifting Focus from Documentation to Data Uncovering the Benefits of Shifting Your Focus From Documentation to Data For Validation leaders,…

Importance of Process Mapping in Kneat Deployment: Beginning with the End in Mind In this on-demand webinar Paul Smith, Partner…

Achieving Computer Software Assurance (CSA) with Digital Validation The FDA recently released its Draft Guidance for Computer Software Assurance (CSA)…

How to Budget for Digital Validation & Maximize ROI Join Derek Hughes, VP US Sales, Kneat, Justin Blackwelder, Project Services…

Discover how Kneat Academy’s professional training programs can help you to increase your productivity, confidence, and competence in Kneat Gx with this webinar presented by Rick Mineo, Kneat Academy Director and Director of Strategic Partnerships.
The ISPE Baseline Guide 5 (Second Edition) provides ‘best of the best’ practical guidance on the implementation of a science and risk-based approach for Commissioning and Qualification (C&Q). Watch this webinar to understand the key principles of ISPE Baseline Guide 5 and how to apply them in a paperless validation environment while exploring the key features and functionality of Kneat.
Understand how this world biotechnology leader with over 45,000 employees and facilities worldwide, globally transformed the productivity of its Commissioning and Qualification processes, using Kneat Gx e-validation software’s automated traceability.
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