Webinars & Events

Cleaning Validation Programmes: Establishing a Compliance-Led Framework

Uncover the essential strategies for building a successful Cleaning Validation program that streamlines compliance and boosts operational efficiency.

Paper to Glass: Exploring the Digital Transition of Logbook Management in Pharma

Discover the key steps to transition from paper to digital logbooks and elevate your life sciences operations.

Digital Transformation

Challenges and Solutions: A Deep Dive Into Digital CQV

Discover how digital transformation in Commissioning, Qualification, and Validation (CQV) can streamline operations, ensure compliance, and equip you to stay ahead in the evolving pharmaceutical and biotechnology landscape.

Commissioning and Qualification (CQV)

Real Time Process Monitoring: Why and How Can You Achieve It

Discover how continued process verification and advanced predictive tools are revolutionizing quality management for safer, more efficient processes.

Moving Beyond Excel: How a Digital Risk Management Tool Is Better for CMC Development

Unlock faster development and streamlined CMC workflows with digital solutions that enhance risk management, collaboration, and regulatory compliance.

ValGenesis Process Manager: The Future of Cleaning Validation

Explore the future of cleaning validation with advancements in digitization and technology, and learn how to overcome traditional challenges while meeting increasingly stringent regulatory expectations with a science- and risk-based approach.

Cleaning Validation

Improving AM Development With a Specialized Risk Management Tool

Discover how integrating a quality risk management tool can revolutionize your analytical methods, overcoming challenges and delivering impactful results.

Quality Risk Management

Out of the Box CSA with ValGenesis VLMS

Discover how CSA can elevate your validation process with modern methodologies and ValGenesis VLMS!

Computer System Validation (CSV)

Computer Software Assurance (CSA)

Common FDA 483 Cleaning Validation Observations and How to Avoid Them

Join our webinar to learn how to overcome the pharmaceutical industry's cleaning validation challenges, avoid FDA Warning Letters, and protect patient safety and product quality.

Digital Validation

Cleaning Validation

CQV: From a Painful Manual Approach to a Smooth Digital Process

Transform your CQV process with ValGenesis VLMS: a seamless digital solution to eliminate manual pain points and streamline your transition to a fully digital environment.

Commissioning and Qualification (CQV)

Digital Validation

A Roadmap to Digitalize Your Control Strategy

Learn essential steps for digitalizing control strategies in the pharmaceutical and biopharmaceutical industries, and explore key concepts and benefits of digital solutions.

Digital Transformation

Process Digitalization

Boost Efficiency and Quality with CSA and Modern Software Tools

Explore how CSA enhances resource allocation and quality, with modern software tools accelerating the validation process.

Computer Software Assurance (CSA)

The Toolbox for an Effective Tech Transfer

Explore how cutting-edge digital tools and Pharma 4.0 methodologies are revolutionizing (bio)pharmaceutical Technology Transfer.

Digital Transformation

Managing Cleaning Validation at an Operational Facility (Hosted by KENX)

Ensuring the validated state of a cleaning process is complex, balancing efficiency, compliance, and constant readiness. This webinar talks about how we cannot only get this balance right by using digital tools.

Cleaning Validation

First Look: VLMS 5.0

Get a first look at ValGenesis VLMS 5.0, the latest milestone release of the industry's leading digital validation solution.

Digital Validation

Avoiding the Pitfalls of APQRs

Digital CPV

What’s Stopping You? Overcoming CSA Adoption Concerns

Computer Software Assurance (CSA)

Beyond Binders: Instant Accessibility to All Your Logbook Data

Electronic Logbook Management

Digital CQV and Pharma 4.0: Paving the Way for Future Success

Commissioning and Qualification (CQV)

Emerging Technology

Pharma 4.0

Facility and Utility Validation

Smart Factories Are Coming: Here’s What You Need To Know

Digital Transformation

Pharma 4.0

Unveiling Key Strategies for Optimizing Quality Risk Management

Quality Risk Management

VLMS is the Best Technical Solution to Implement CSA Guidance

Computer Software Assurance (CSA)

Application of Digital Twin Using Process Analytics

Digital Twin

Best Practices in Commissioning and Qualification

Commissioning and Qualification (CQV)

Facility and Utility Validation

Risk Management of Biopharma Operations Over Lifecycle - An ICH Q12 Overview

Quality Risk Management

Process Digitalization

Post-Approval Changes

Digital Transformation in CDMOs: Streamlining Tech Transfer Processes

Digital Transformation

Integrating ValGenesis iRisk with Process Insight to Address Subjectivity

Digital CPV

Quality Risk Management

Digital CPV: Important Step in Your Pharma 4.0 Journey

Digital CPV

Pharma 4.0

An Intro to ValGenesis e-Learning: Join the ValGenesis University Coffee Chat

Establishment of a Digital QRM Program Using ValGenesis iRisk

Quality Risk Management

ValGenesis e-Logbook: Mastering Logbook Operational Compliance

Electronic Logbook Management

Discover the Digital CPV Revolution!

Digital CPV

Discover Step-By-Step CSA Implementation With ValGenesis VLMS

Watch how ValGenesis VLMS applies a risk-based approach to requirements for out-of-the-box CSA.

Computer Software Assurance (CSA)

Digital Cleaning Validation Lifecycle

The industry has moved toward a structured, risk-based lifecycle approach following FDA's Process Validation Lifecycle guidance. See how to automate and digitize your cleaning validation with purpose-built tools.

Cleaning Validation

Join the Digital CPV Revolution With Process Insight!

Digital CPV

Data-Driven Risk Management: a Practical Approach to Minimize Subjectivity

Quality Risk Management

6 T’s to CSA Adoption

Explore what's needed to successfully adopt CSA in your organization.

Computer Software Assurance (CSA)

The Path to Real-time CPV: An Implementation Case Study

Digital CPV

Diving Into the Nexus of Life Sciences and Next-Gen AI

Pharma 4.0

For OEMs: Drive New Agility in Qualification Service Requests

Commissioning and Qualification (CQV)

How to Meet Efficiency and Compliance in Equipment Qualification

Commissioning and Qualification (CQV)

Effective Deployment of Quality Risk Management

Quality Risk Management

Understanding Digital Validation: How Does It Work?

Digital Validation

Digitization of Cleaning Validation Life Cycle

Cleaning Validation

How to (Really) Calculate the ROI of Digitized Validation

Digital Validation

How to Manage Logbooks Electronically

See how to quickly capture equipment info in an electronic logbook, convert paper forms to digital versions, define verification and approval business rules, capture log entries without an internet connection, and more.

Electronic Logbook Management

Introducing VLMS 5.0: An Introduction for Partners

Watch the short webinar introducing the new features of VLMS 5.0.