Pharma eLearning that gets through medical, legal, and regulatory review
SOP, product, and compliance training for life-sciences teams – scripted from your approved source material, planned around your review cycle, and localized for every market you launch in.
In pharma, review takes as long as development
Life-sciences training has to be engaging and accurate at the same time. A single unapproved claim in a product module can hold up a launch. An SOP course that doesn't match the current SOP version can create problems at audit.
Common pressures we hear from pharma L&D and medical training teams:
Medical, legal, and regulatory reviewers who each need their own pass
SOP updates that leave existing courses out of date
Global launches that need the same course in many languages, all at once
Field teams who need short, practical product refreshers – not hour-long modules
Proving who completed what, and when
Courses for the entire product lifecycle
SOP and GxP-awareness training
Step-by-step modules and knowledge checks aligned with your controlled documents
Product and disease-area training
Mechanism-of-action animations, interactive case scenarios, and sales enablement for field teams
Compliance training
Code-of-practice, pharmacovigilance awareness, and anti-bribery modules, complete with assessments
Onboarding programs
For new starters in manufacturing, quality, commercial, and medical roles
Microlearning and interactive video
Short refreshers for reps and medical science liaisons
Rapid conversion
Approved slide decks and PDFs converted into interactive, SCORM-ready courses
Built around your review and compliance processes
Much of our work supports medical and life-sciences training. We know your reviewers set the timeline – so we plan every project around them.
We write from the references you provide and cite them in the storyboard, so reviewers can verify every claim.
Medical, legal, and regulatory reviewers sign off on the storyboard before development begins – reducing rework at alpha and beta.
Localize a2z is certified to ISO 9001:2015 and ISO 13485:2016, helping us maintain a disciplined approach to quality.
Your quality and regulatory teams keep final approval. We provide the course files, SCORM tracking, and documentation they need.
Through Localize, we handle translation and voice-over under ISO 17100:2015, with 100+ native voice artists.
Relevant services
Regulated training moves faster when development, conversion, and localization sit with one team and one review process.
Not sure which fits? Tell us about your project and we'll recommend the right mix.
- Custom eLearning developmentCourses designed and written from your material, built in Storyline, Rise, or HTML5
- eLearning localizationTranslation, native voice-over, and QA in every language you need
- Interactive video and animationBranching video, explainer animations, and scenario clips
- Rapid PowerPoint-to-eLearning conversionSlide decks and PDFs transformed into interactive, trackable courses
- Medical devicesDevice, procedure, and service training for clinical and field teams
Experience with international pharmaceutical companies
We have developed eLearning for international pharmaceutical companies. Localize a2z supports life-sciences clients with translation and localization.
Frequently asked questions
Can you work with our medical, legal and regulatory review process?
Yes. We build review rounds into the timeline from the start, and reviewers approve the storyboard before development begins.
Are your courses GxP validated?
We don't validate courses on your behalf – validation belongs to your quality system. We develop courses that support your review and compliance processes, and provide the files and tracking your team needs.
Can you update courses when an SOP changes?
Yes. Tell us what changed, and we'll scope the update. Developing in Rise, or planning modular Storyline files, helps keep updates quick.
Can the same course launch in several countries?
Yes. Through Localize, we translate the on-screen text, record native or human-reviewed AI voice-over, and run linguistic QA.
Planning a launch or an SOP refresh?
Send us your source material and review route, and we'll come back with a development plan that fits.