SOLUTIONS / MULTIMEDIA & E-LEARNING
Trained patients. Reliable data.
A patient-training package for clinical trials: one instructional film or animation, localized into every language you run, plus an e-learning check that confirms each participant understood — before the first data point.
HOW IT WORKS — ONE COORDINATED PROVIDER
01
We scope it & send one quote
02
You approve the script & storyboard
03
We produce & localize
04
We deploy on your LMS or ours
05
Go live — with reporting
DELIVERED IN YOUR MARKETS
English
Español
Deutsch
Français
Italiano
Polski
日本語
+ 250 language pairs
WHAT’S INSIDE
One package. The whole training chain.
You hand us what the participant needs to learn — a device, a medication, a protocol. We hand you a deploy-ready training kit: no in-house studio, no juggling four vendors, no translation guesswork.
Instructional film or animation
Produced from scratch to medical standards — live-action or animation, whichever fits the device. Patient-friendly or clinical.
Localized into every language
Native voice-over, synced subtitles and localized on-screen text — validated by the same team trusted for our regulatory content.
E-learning + deployment
An interactive, scored module that confirms the participant can do it right — deployed on your LMS or ours, with completion records, certificates and reporting.
Compliance built in
IFU-aligned messaging, persistent training disclaimer, no identifiable patients, GDPR by design. Source files kept for change control.
Two audiences. One production.
Same device or protocol, different viewers. We tune tone, depth and the knowledge check to whoever needs to get it right — often both, from a single production.
Patients
At-home & decentralized use
• Plain-language, reassuring walkthrough of first use
• Fewer support calls and mis-readings from home
• Higher compliance = cleaner data from every participant
• Delivered in the patient’s own language
Site & medical staff
Sites, nurses, trial coordinators
• Standardized training across every site
• Record readings per protocol & site SOPs, consistently
• Competency check = auditable proof of training
• Faster site activation, less re-training
CERTIFICATIONS & COMPLIANCE
Training that survives an audit.
The same certified processes we’ve applied to regulatory documentation for over 25 years.
ISO 9001:2015
Certified quality management
ISO 17100:2015
Certified translation & localization
3rd place
EMA e-learning tender
MDR-aligned & GDPR
Secure by design
WHY SPONSORS CARE
A participant who doesn’t understand is unreliable data.
Every unclear reading, every mis-used device at home is a protocol deviation waiting to happen. This package removes that variable at the source.
8/10
The team CROs already trust
8 out of 10 top global CROs trust KONTEKST with clinical content.
99.8%
Delivered on time
The on-time record you already know from our regulatory work — applied to your training assets.
25+
Years of experience
Over 25 years supporting life sciences with regulated content — now packaged into one training solution.
Have a study? We’ll have your participants trained, in every language.
Send us the device, medication or protocol and the IFU. We’ll come back with a scoped plan and a fixed quote — usually within days.