KENX Clinical Program
A complete program for clinical operations and clinical trials.
A decade of GxP quality and compliance training, now extended into clinical development. From what regulators expect of AI in trials to operationalizing ICH E6(R3), built for the people accountable for quality, data, and GCP.
- Six free live webinars running through January 2027
- AI in Clinical Operations & Clinical Trials , our 2027 flagship conference
- Clinical Quality & GCP University , launching 2027
Who we are
10
Years serving
GxP compliance
GxP compliance
15+
Conferences
every year
every year
5
Countries and
territories
territories
KENX has spent a decade convening the life sciences quality and compliance community. We are bringing that same discipline to clinical development.
Join the program
One form keeps you connected to everything, the full webinar series and first word on our 2027 conferences. Tell us what to send.
By signing up you agree to receive communications from KENX. Unsubscribe anytime.The webinar series
Six live panels. Free to attend.
Practitioner panels working through where artificial intelligence is reshaping clinical trials, and what it demands of the people responsible for quality, data, and compliance.
1
AI in Clinical Trials: What FDA and EMA Now Expect
Aug 6, 2026
2
Validating AI and ML in Clinical Systems: Extending CSA to GCP
Sep 10, 2026
3
AI in Clinical Data Management: Automation, Reconciliation, and Data Integrity
Oct 27, 2026
4
AI Driven Patient Recruitment and Site Selection
Nov 12, 2026
5
Centralized and Risk Based Monitoring with AI
Dec 3, 2026
6
Generative AI for Protocols, CSRs, and Regulatory Narratives
Jan 14, 2027
Launching 2027
Two conferences. One clinical vertical.
One event follows the technology. The other builds the discipline. Sign up above to be first to know when dates, agendas, and early rates are released.
2027 · Flagship
AI in Clinical Operations & Clinical Trials
Two days across the full clinical lifecycle: regulatory expectations, validating AI in clinical systems, data management and integrity, patient recruitment and site selection, risk based monitoring, and generative AI for clinical and regulatory writing.
2027 · New
Clinical Quality & GCP University
ICH E6(R3) is the most significant revision to GCP in decades, and every sponsor and CRO now has to operationalize it. Two days on inspection readiness, GCP auditing, CRO and vendor oversight, and building a clinical quality system that holds up when the regulator arrives.
Built for
Who this is for.
The people accountable when AI touches a trial, across quality, data, operations, and regulatory.
Clinical Operations
Clinical Quality Assurance
GCP Compliance & Auditors
Clinical Data Management
Biometrics
Regulatory Affairs
Medical Writing
CSV / CSA
Clinical Systems
Safety & Pharmacovigilance
