Knowledge Exchange Network
KENX is dedicated to making the life science industry safer through knowledge exchange, training, and community support. With a history rooted in FDA and globally-regulated environments, they focus on providing tools, techniques, and educational opportunities such as conferences, webinars, and publications to enhance industry practices. Their mission is to connect professionals, foster innovation, and promote compliance and quality in regulated industries.
Industries
Nr. of Employees
small (1-50)
Knowledge Exchange Network
Products
CSV/CSA University Compendium
Recorded curriculum and presentation compendium covering computer system validation and computer software assurance topics for regulatory compliance.
Validation University Europe Compendium
On-demand recorded content from a Europe-focused validation curriculum intended for validation and quality professionals.
QRM Virtual Toolkit
A packaged on-demand set of QRM training videos and practical tools providing several hours of instruction on quality risk management implementation.
CSV/CSA University Compendium
Recorded curriculum and presentation compendium covering computer system validation and computer software assurance topics for regulatory compliance.
Validation University Europe Compendium
On-demand recorded content from a Europe-focused validation curriculum intended for validation and quality professionals.
QRM Virtual Toolkit
A packaged on-demand set of QRM training videos and practical tools providing several hours of instruction on quality risk management implementation.
Services
Multi-day events covering topics such as sterility assurance, medical device validation, GMP modernization, outsourcing, CSV/CSA, and AI in GxP. Events are offered with virtual attendance options.
Short-form webcasts and longer recorded sessions on GMP inspections, contamination control, AI in validation, CSV/CSA, validation documentation, and related topics.
On-demand training series such as a Quality Risk Management toolkit that provides multi-hour instruction and practical tools for implementing QRM.
Subscription access to a content library containing SOPs, templates, checklists, training videos, and related compliance tools.
Commercially available compendia and recordings of conference presentations for asynchronous review and continuing education.
Peer-review process and editorial oversight for publishing articles and thought leadership on corporate compliance and life sciences regulation.
Multi-day events covering topics such as sterility assurance, medical device validation, GMP modernization, outsourcing, CSV/CSA, and AI in GxP. Events are offered with virtual attendance options.
Short-form webcasts and longer recorded sessions on GMP inspections, contamination control, AI in validation, CSV/CSA, validation documentation, and related topics.
On-demand training series such as a Quality Risk Management toolkit that provides multi-hour instruction and practical tools for implementing QRM.
Subscription access to a content library containing SOPs, templates, checklists, training videos, and related compliance tools.
Commercially available compendia and recordings of conference presentations for asynchronous review and continuing education.
Peer-review process and editorial oversight for publishing articles and thought leadership on corporate compliance and life sciences regulation.
Expertise Areas
- Regulatory compliance training (GMP, inspections, enforcement)
- Computer system validation and computer software assurance (CSV/CSA)
- Validation lifecycle and documentation practices
- Sterility assurance and contamination control
Key Technologies
- Artificial intelligence / machine learning (applied to validation and process optimization)
- Computer system validation (CSV) methodologies
- Computer software assurance (CSA) methodologies
- Quality risk management (QRM) tools and methods
News & Updates
Explore KENX's 2025 conference schedule to plan training, speaking, and sponsorship opportunities.
In-person conferences in Philadelphia and San Diego focusing on sterility, microbiology, and validation.
Educational events in San Diego and Philadelphia on GMP, validation, and digital tools.
Validation principles from A to Z in Dublin, Ireland.
Training on compliance and integrity across traditional, digital, and AI-driven systems.
Discusses the challenges of data security and integrity in digital change within the pharmaceutical industry.
Explore KENX's 2025 conference schedule to plan training, speaking, and sponsorship opportunities.
In-person conferences in Philadelphia and San Diego focusing on sterility, microbiology, and validation.
Educational events in San Diego and Philadelphia on GMP, validation, and digital tools.
Validation principles from A to Z in Dublin, Ireland.
Training on compliance and integrity across traditional, digital, and AI-driven systems.
Discusses the challenges of data security and integrity in digital change within the pharmaceutical industry.