Take Advantage of Early Bird pricing through July 16th!
Join KENX for hands-on training for engineering, quality, C&Q and validation professionals within the pharmaceutical, biotech, medical device and related industries. Participants can create-their-own-experience by choosing from over 55 tutorials and benefit from the wealth of knowledge and useful material our faculty exchanges. Val-U offers a hands-on experience in which lessons learned turn into immediate, actionable results.
55 Tutorials Overflowing with Rich Content and Tangible Takeaways for the CQV Universe
Facility Commissioning & Equipment Qualification
Implement a Risk-based Verification Strategy
Design a Risk-based IQ, OQ, and PQ Approach
Manage Process Validation Tech Transfers
Qualify Critical Utility Systems – HVAC, Water and Gas
Learn How To Use Statistics in Validation – Statistics for Non-Statisticians
Implement a 3-Stage Process Validation Approach
Master the Validation Master Plan (VMP)
Conduct Risk-based Continued Process Verfications
Understand Key Elements to a Successful Program
Establish Cleaning Residue Limits and Acceptance Criteria
Establishing Bioburden and Endotoxin limits for Sterile and Non-sterile Products and Processes
Receive a Cleaning Validation Assessment Checklist Example
Computer System Validation
Stay up to speed with FDA’s Computer Software Assurance proposed draft
Implement a Risk-Based CSV Program Enterprise-Wide
Develop and Validate SAAS, IAAS, and Other Software Programs
Qualify Network Infrastructure and Cloud Environments
Personnel In The Following Environments Should Attend:
Regulatory and Compliance
This event is also appropriate for business development and sales managers that offer innovative solutions for quality, validation and engineering professionals in the life science environment.
Simply fill out this form below to register for the conference. KENX will arrange invoicing and will provide you with a log-in to the virtual platform and in-person details.