We're transforming how pharmaceutical companies create training content. Our mission is to bridge the gap between rapid innovation and rigorous compliance, enabling teams to produce audit-ready courses in minutes instead of months.
Our platform is built on three core pillars that address pharmaceutical L&D's most pressing needs.
Radically reduce the time required to create and update validated GxP, SOP, and product training materials—from a scale of months to hours.
Generate training content with a built-in, immutable audit trail that provides complete traceability from source document to final SCORM package.
Empower subject matter experts to create accurate, engaging, and consistently up-to-date training that improves critical role performance.
Compliance isn't an add-on—it's woven into our platform architecture from day one.
Electronic records and signatures that meet FDA requirements. Secure audit trails, access controls, and system validation documentation included.
Supports GMP, GCP, and GLP training requirements. Every course is documented and validated to meet regulatory inspection standards.
Every action is logged with timestamps, user identification, and change history. Complete traceability from source to course content.
Enterprise-grade security with encrypted data at rest and in transit, role-based access controls, and multi-tenant data isolation.
Trusted by L&D and Medical Affairs teams across the life sciences industry.
Global pharma leaders using Medimpacto to train sales reps, MSLs, and compliance teams.
Innovative biotech firms accelerating scientific training for rapid product launches.
Device manufacturers ensuring field teams understand complex product protocols.