Webinars

AI Powered Validation: How to be Smarter, Faster, and More Reliable

Artificial Intelligence (AI)

Digital Validation

Emerging Technology

Reducing Errors and Gaining Efficiency in Your CPV

Digital CPV

Revolutionizing CMC: Cutting Errors and Delays in Quality by Design

Learn how pharma teams are overcoming common QbD challenges with practical strategies and digital tools that make implementation faster and more reliable.

Quality by Design (QbD)

Meet VAL and Take Advantage of AI-Driven Validation

Discover how VAL, the AI-powered Validation Assistant, is transforming outdated, error-prone validation into a faster, smarter, and more compliant process.

Artificial Intelligence (AI)

Digital Validation

Introducing ValGenesis Validation Lifecycle Suite

Step into the future of digital validation with ValGenesis VLS - our all-in-one, AI-powered suite for better execution and maximum efficiency.

Artificial Intelligence (AI)

Computer Software Assurance (CSA)

Computer System Validation (CSV)

Cleaning Validation

Commissioning and Qualification (CQV)

No More Manual Bottlenecks: Streamline Compliance and Free Up Resources

Explore how digital, automated CPV eliminates manual inefficiencies, enables early signal detection, and strengthens proactive quality management across pharma and biomanufacturing.

Digital CPV

Avoid CPV Failures: Proven Ways to Catch Deviations Early

Discover how modern CPV strategies can transform compliance from reactive reviews into a proactive, real-time early-warning system that safeguards quality and minimizes risk.

Digital CPV

Preventing Rework Through Intelligent, Real-Time Error Detection

Cut costly delays and regulatory risks in CQV projects — see how intelligent, paperless validation software reduces rework by detecting errors in real time and accelerating compliance.

Artificial Intelligence (AI)

Commissioning and Qualification (CQV)

Introducing ValGenesis Process Lifecycle Suite

Discover how ValGenesis Process Lifecycle Suite is transforming life sciences with a unified digital platform that drives efficiency, compliance, and quality across the entire process lifecycle.

Quality Risk Management

Digital CPV

Quality by Design (QbD)

Why is Manual Validation Holding you Back? The Evolution of AI-Driven Validation in Regulated Industries

Discover how AI-powered validation is transforming slow, error-prone manual processes into faster, smarter, and fully compliant workflows.

Artificial Intelligence (AI)

Digital Validation

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

Discover how digital CQV is transforming manual documentation burdens into streamlined, compliant processes—accelerating your path to Pharma 4.0.

Pharma 4.0

Commissioning and Qualification (CQV)

Emerging Technology

Facility and Utility Validation

Achieving Regulatory Readiness: How to Minimize Audit Stress

Join our webinar to see how ValGenesis Smart GxP™ helps pharma leaders slash audit prep time by 70%, cut validation cycles by 80%, and reduce observations by 90%—turning compliance into a competitive edge.

Artificial Intelligence (AI)

Digital Validation

Redefining Compliance: Benefits of Running CPV in Real Time

Discover how digital CPV is transforming compliance into a competitive advantage by centralizing data, enhancing process control, and accelerating pharmaceutical digital transformation.

Digital CPV

Digital Transformation

Reimagining Tech Transfers: How Automation and AI Assessments Deliver Smoother Processes

See how AI and automation are streamlining processes, boosting collaboration, and driving faster, more confident decisions in pharma and biotech.

Artificial Intelligence (AI)

Pharma 4.0

Revolutionizing CMC in Drug Development: How to Reduce Errors and Delays in Quality by Design

Power up your QbD journey with integrated tools that enhance collaboration, data integrity, and risk management.

Quality by Design (QbD)

Manufacturing Bottlenecks: Why Analog Cleaning Validation Programs Slow Down Your Entire Operation

Struggling with paper-based cleaning validation? Go digital to simplify compliance, accelerate batch release, and maximize operational efficiency.

Cleaning Validation

AI and Machine Learning as Enablers for Industry 4.0

Explore how AI and machine learning are transforming pharma and biotech manufacturing - from smarter validation to real-time process control and continuous improvement.

Artificial Intelligence (AI)

Machine Learning (ML)

Best Practices in Commissioning and Qualification

Discover how an integrated C&Q approach can streamline processes, reduce costs, and accelerate your path to compliance.

Commissioning and Qualification (CQV)

Facility and Utility Validation

Inspection-Ready Validation: Strategies for a Seamless Regulatory Audit

Discover how ValGenesis VLMS transforms inspection challenges into opportunities for streamlined compliance and operational excellence in the life sciences industry.

Digital Validation

Digitize with Precision: Mastering Carry Over Calculations in Cleaning Validation

Transform cleaning validation from an afterthought to a streamlined, digital process that ensures compliance and minimizes risks!

Vendor Testing in VLMS: The Value of PDF Execution

Struggling with PDF-based Operational Qualification documentation? Discover how ValGenesis transforms equipment qualification into a seamless, digital experience.

Digital Validation

Digital Transformation of Your Site: A Step-By-Step Program

Discover how digital transformation is revolutionizing pharma and biopharma, enabling smarter manufacturing, streamlined regulatory pathways, and accelerated product lifecycles.

Pharma 4.0

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.

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 iVal: 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

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

VLMS is the Best Technical Solution to Implement CSA Guidance

Computer Software Assurance (CSA)

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

Digital CPV: Important Step in Your Pharma 4.0 Journey

Digital CPV

Pharma 4.0

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

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)

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