Webinars & Events
ValGenesis sponsors, attends, and presents at conferences all over the world. In addition, we host a regular series of thought leadership webinars covering what's important for GxP organizations.
Wednesday, December 11
Cleaning Validation Programmes: Establishing a Compliance-Led Framework
Kenneth Pierce
Director of Product, Process & Cleaning Validation Lifecycle
Computer Software Assurance (CSA)
Emmanuel Cansino
Senior Director Industry Solutions
Title | Presenter | Link |
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Coming Soon! Wednesday, December 11
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. |
Kenneth Pierce Director of Product, Process & Cleaning Validation Lifecycle |
Register |
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 |
Yowvanaraj Gopal Director Professional Services |
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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) |
Sachin Maled Senior Manager - Presales |
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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. |
Sandra Silva Director, Product Management - CPV |
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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. |
Margarida Ventura Senior Consultant |
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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 |
Rui Almeida Director - Consulting Services |
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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 |
Margarida Ventura Senior Consultant |
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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) |
Jeff Ramos Solutions Engineer |
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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 |
Sachin Maled Senior Manager - Presales |
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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 |
Sandeep Lakshmanan Sr. Project Manager |
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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 |
Daniel Pais Senior Consultant |
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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) |
Emmanuel Cansino Senior Director Industry Solutions |
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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 |
Rui César Silva Senior Consultant |
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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 |
Saurabh Joshi Director - Industry Solutions |
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Get a first look at ValGenesis VLMS 5.0, the latest milestone release of the industry's leading digital validation solution. Digital Validation |
Sophia Vraka Senior Solutions Engineer |
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Avoiding the Pitfalls of APQRs Digital CPV |
Rui Almeida Director - Consulting Services |
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What’s Stopping You? Overcoming CSA Adoption Concerns Computer Software Assurance (CSA) |
Jeff Ramos Solutions Engineer |
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Beyond Binders: Instant Accessibility to All Your Logbook Data Electronic Logbook Management |
Sathish Kumar Shanmugam Global VP of Customer Advocate |
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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 |
Saurabh Joshi Director - Industry Solutions |
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Smart Factories Are Coming: Here’s What You Need To Know Digital Transformation Pharma 4.0 |
Ângela Martinho Vice President, Consulting Services |
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Unveiling Key Strategies for Optimizing Quality Risk Management Quality Risk Management |
Margarida Ventura Senior Consultant |
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VLMS is the Best Technical Solution to Implement CSA Guidance Computer Software Assurance (CSA) |
Emmanuel Cansino Senior Director Industry Solutions |
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Application of Digital Twin Using Process Analytics Digital Twin |
Maria Batalha Consultant |
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Best Practices in Commissioning and Qualification Commissioning and Qualification (CQV) Facility and Utility Validation |
Saurabh Joshi Director - Industry Solutions |
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Risk Management of Biopharma Operations Over Lifecycle - An ICH Q12 Overview Quality Risk Management Process Digitalization Post-Approval Changes |
José C. Menezes CSO |
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Digital Transformation in CDMOs: Streamlining Tech Transfer Processes Digital Transformation |
Rui César Silva Senior Consultant |
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Integrating ValGenesis iRisk with Process Insight to Address Subjectivity Digital CPV Quality Risk Management |
Margarida Ventura Senior Consultant |
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Digital CPV: Important Step in Your Pharma 4.0 Journey Digital CPV Pharma 4.0 |
Saurabh Joshi Director - Industry Solutions |
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An Intro to ValGenesis e-Learning: Join the ValGenesis University Coffee Chat |
Nancy Cattle Vice President, Learning Services |
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Establishment of a Digital QRM Program Using ValGenesis iRisk Quality Risk Management |
Ricardo Leandro Group Product Manager - Risk |
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ValGenesis e-Logbook: Mastering Logbook Operational Compliance Electronic Logbook Management |
Anthony Manzanares Industry Solutions Engineer |
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Discover the Digital CPV Revolution! Digital CPV |
Sandra Silva Director, Product Management - CPV |
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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) |
Sophia Vraka Senior Solutions Engineer |
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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 |
Rui Almeida Director - Consulting Services |
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Join the Digital CPV Revolution With Process Insight! Digital CPV |
Sandra Silva Director, Product Management - CPV |
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Data-Driven Risk Management: a Practical Approach to Minimize Subjectivity Quality Risk Management |
Margarida Ventura Senior Consultant |
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Explore what's needed to successfully adopt CSA in your organization. Computer Software Assurance (CSA) |
Emmanuel Cansino Senior Director Industry Solutions |
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The Path to Real-time CPV: An Implementation Case Study Digital CPV |
Maria Batalha Consultant |
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Diving Into the Nexus of Life Sciences and Next-Gen AI Pharma 4.0 |
Steve Thompson Senior Director Product Marketing |
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For OEMs: Drive New Agility in Qualification Service Requests Commissioning and Qualification (CQV) |
Sachin Maled Senior Manager - Presales |
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How to Meet Efficiency and Compliance in Equipment Qualification Commissioning and Qualification (CQV) |
Saurabh Joshi Director - Industry Solutions |
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Effective Deployment of Quality Risk Management Quality Risk Management |
Joana Brito QRM Specialist |
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Understanding Digital Validation: How Does It Work? Digital Validation |
Emmanuel Cansino Senior Director Industry Solutions |
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Digitization of Cleaning Validation Life Cycle Cleaning Validation |
Sunil Patel Director - Product Management |
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How to (Really) Calculate the ROI of Digitized Validation Digital Validation |
Emmanuel Cansino Senior Director Industry Solutions |
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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 |
Sophia Vraka Senior Solutions Engineer |
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Introducing VLMS 5.0: An Introduction for Partners Watch the short webinar introducing the new features of VLMS 5.0. |
Watch |