VIEW UPCOMING CONFERENCES
KENX conferences will now be offered both virtually and in-person (depending on federal/local regulations and corporate travel restrictions). This hybrid model allows you to choose how you would like to attend our events.
IN-PERSON & VIRTUAL CONFERENCES
135 E Kings Highway
3rd Floor
Haddonfield, NJ 08033
Email: info@kenx.org
Phone: 858 649 3251
VALIDATION AND GMP UNIVERSITY
August 24 – August 26
Virtually
Knowledge Exchange Network (KENX) is very excited to announce Validation University is returning to Philadelphia. The event is a dream come true for engineering, quality, C&Q and validation professionals by offering hands-on training for the pharmaceutical, biotech, medical device and related industries.
PROCESS VALIDATION & CONTINUED VERIFICATION
August 24 – August 26
Virtually
Process Validation is the backbone of all validation and is always under FDA regulatory scrutiny. KENX is excited to announce the definitive process validation and continued process verification conference of 2019…
DATA INTEGRITY INSPECTION READINESS SUMMIT
August 24 – August 26
Virtually
Data Integrity remains the life science industry’s greatest challenge as Warning Letters continue to rise year-over-year. These serious findings include; having interrupted, missing, deleted and lost data; inadequate records for risk analysis; failure to exercise appropriate controls; failure to validate computer software; failure to establish validation procedures; manipulation and deletion of audit trails; and many more…
LABORATORY UNIVERSITY
October 5 – October 7
Virtually or in San Diego, United States
Laboratory University contains 3 amazing events at one location! Create your own event by choosing from over 40 knowledge exchanges tutorials, including…
ANALYTICAL PROCEDURES & METHODS VALIDATION
October 5 – October 7
Virtually or in San Diego, United States
The time has never been greater to stay up-to-speed with current regulatory thinking. Between FDA’s interest in releasing guidance’s the last few years on Analytical Procedures & Methods Validation, Bioanalytical Methods Validation and a flurry of global regulations on data integrity, it is critical for you and your company to receive the training you need…
STABILITY TESTING & PROGRAM MANAGEMENT
October 5 – October 7
Virtually or in San Diego, United States
Stability testing is critical to the efficacy of drug substances. ICH, FDA and WHO stability guidance’s have been around for quite some time and are strictly enforced, however, industry still has challenges to overcome and seeks more direction…
LABORATORY DATA INTEGRITY
COMPLIANCE CONGRESS
October 5 – October 7
Virtually or in San Diego, United States
Most data integrity non-compliance are cited in the GMP laboratory. These serious findings include; having interrupted, missing, deleted and lost data; inadequate records for risk analysis; failure to exercise appropriate controls; failure to validate computer software; failure to establish validation procedures; manipulation and deletion of audit trails; and many more…
COMPLIANCE CONGRESS
VALIDATION UNIVERSITY EUROPE
November 23 – November 25
Virtually or in Dublin, Ireland
Knowledge Exchange Network (KENX) is very excited to announce their Validation University is returning to Ireland this fall. The event is a dream come true for engineering, quality, C&Q and validation professionals by offering hands-on training for the pharmaceutical, biotech, medical device and related industries…
COMPUTER SYSTEMS VALIDATION
& DATA INTEGRITY INSPECTION READINESS
November 23 – November 25
Virtually or in Dublin, Ireland
MHRA, FDA and many other global regulations have issued many guidance’s regarding Data Integrity. How does one navigate this maze? Moreover, as data integrity matures and malicious threats have become commonplace, what do you do next?
& DATA INTEGRITY INSPECTION READINESS
PROCESS VALIDATION & CONTINUED PROCESS VERIFICATION
November 23 – November 25
Virtually or in Dublin, Ireland
Process Validation is the backbone of all validation and is always under FDA regulatory scrutiny. KENX is excited to announce the definitive process validation and continued process verification conference of 2019. This event gives you the tools and technology needed to create, deploy and maintain best practices through all three stages of validation…
CLEANING VALIDATION & CRITICAL CLEANING PROCESSES
November 23 – November 25
Virtually or in Dublin, Ireland
A compliant cleaning validation program is essential for a successful regulatory inspection. Even today, many have struggled to develop effective processes and keep up with evolving sterile regulations that meet an inspector’s expectations…
COMPUTER SYSTEMS VALIDATION & DATA INTEGRITY COMPLIANCE CONGRESS
December 7 – December 9
Virtually or in Philadelphia, PA, United States
This fall, FDA plans to release a draft guidance on Computer Software Assurance! Are you prepared? To this day, CSV and Data Integrity challenges remain high in our rapidly changing environment. In fact, FDA and other regulators continue to find serious findings including; having interrupted, missing, deleted and lost data; inadequate records for risk analysis; failure to exercise appropriate controls; failure to validate computer software; failure to establish validation procedures; manipulation and deletion of audit trails; and many more…