Training built around your team, not a calendar.
Tell us what your group needs to master, from GMP and CSV/CSA to data integrity and inspection readiness, and we'll scope a program around your products, processes, and gaps. On-site or virtual.
We reply within one business day. No obligation.
Built from the curriculum behind our international conferences.
AI in GxP
GMP
CSV / CSA
Validation
Data Integrity
Inspection Readiness
Trusted by quality and compliance teams at top pharma, biotech, and MedTech companies.
30+
Years in GxP education
Three decades training pharma, biotech, and MedTech teams on the compliance topics that matter most.
100%
Tailored to your team
We shape the agenda, depth, and case studies around your products, processes, and current gaps.
2
Ways to deliver
Bring our faculty on-site or run it live virtual, for one team or several across multiple sites.
What we train teams on
Pick your topics. We build the depth around your team.
Drawn from the same faculty and curriculum behind our international conferences. Mix several or go deep on one. Your team leaves able to do the work, not just describe it.
GMP Compliance
CSV & CSA
AI in GxP
Sterility Assurance
Laboratory Compliance
Supply Chain & Serialization
MedTech Validation
Data Integrity
Inspection Readiness
Face an audit with confidence
Your team walks into the next FDA or notified-body inspection knowing what's expected and how to respond.
Apply CSA, not just understand it
Validation staff leave with a risk-based approach they can put to work on real systems the following week.
Close gaps specific to your processes
Case studies use your products and workflows, so the training transfers directly to the job.
How it works
A scoped program in four steps.
No open-ended engagements. You'll know the agenda, faculty, and timeline before anything is booked.
1
Tell us your gaps
Share your team, topics, and where the current skills fall short. Takes about two minutes.
2
We scope it
Within one business day we send a draft agenda, faculty match, and delivery options for your group.
3
You approve
Adjust depth, dates, and format until the program fits. No commitment until you sign off.
4
We deliver
On-site or live virtual, across one location or several. Your team leaves job-ready.
Who teaches it
Distinguished faculty, drawn from the field.
Your program is led by the same experts behind our international conferences. They are practitioners and former regulators with backgrounds at leading pharma, biotech, and MedTech organizations, each distinguished in their own area, so your team learns from people who have actually done the work.
Former regulators & inspectors
Agency experience
Faculty who spent careers on the agency side of the table teach your team what inspectors actually look for, and how to be ready long before they arrive.
Industry validation & engineering leaders
Leading life-science companies
Specialists who have spent decades inside top pharma, biotech, and MedTech organizations building, qualifying, and defending real GxP systems, not reading from generic slides.
Quality, data integrity & compliance practitioners
Hands-on in the field
Experts who have built quality systems and stood behind them in audits at major life-science companies, bringing case studies grounded in work that looks like your own.
In their words
What teams say after training with KENX.
We needed to bring a team of 40+ up to speed on CSA, and KENX didn't hand us a generic deck. They built the sessions around our own systems and validation backlog, so people left applying the risk-based approach the same week. Our reviews are leaner and the team is far more confident heading into audits.
Director, CSV & CSA
I run a large team scattered across the US and overseas, so we needed virtual training that worked for everyone, everywhere. KENX was the first call I made, and we had the program scoped in three weeks and delivered within seven. Pulling that together across time zones couldn't have been easier.
VP, Global Quality & Compliance
Start the conversation
Tell us what your team needs.
Share a few details and we'll follow up to scope a program that fits your team and timeline.
We reply within one business day, with a draft agenda, not a sales pitch.
No obligation and no cost to scope. You only commit once you approve.
Program inquiry2 MIN
No spam. Your details are used only to scope your program.
