GRAFX CO. creates MOA and MOD animations, product visualization, and training video assets built for regulated review cycles. We plan around MLR workflows, ISI protocols, and claims-sensitive language so teams can move forward with confidence.
What we produce
We produce premium medical and scientific content for healthcare startups, established brands, and pharma agencies supporting medical clients.
- MOA animations (oncology emphasis): Mechanism of Action storytelling designed for scientific accuracy and clear communication
- MOD animations: Mechanism of Disease narratives that support education and context
- Product visualization films and demos: Clear product representation for launch, web, and stakeholder presentations
- Sales enablement and physician training videos: Assets designed for commercial teams and HCP-facing environments
- Conference, investor, and web explainer variations: Modular outputs tailored for decks, booths, websites, and internal presentations
Creative Innovation. Global Execution.
Headquartered in Manhattan, New York, and Austin, Texas, GRAFX operates a world-class, remote-first production network with specialized hubs in Istanbul and India. This allows us to provide “Follow-the-Sun” Post-Production, Visual Effects execution, 2D/3D animation, and motion design, ensuring your project never stops moving.
Compliance-ready process
Compliance is not a checkpoint at the end. It is how we structure the work from day one.
MLR-friendly workflow
- Review rounds planned into the schedule with clear decision points
- Claims tracking and change logs aligned to stakeholder feedback
- Reference discipline to support scientific statements and sensitive language
Script development with careful language
- Language planned around indication, labeling, and safety requirements
- Fair balance considerations are built into the structure and pacing, where applicable
- Clear separation of on-label content vs off-label risk areas through review gating
Version control and audit trail mindset
- Version naming conventions for review clarity
- Master file management for final delivery and re-use
- Audit-friendly organization for regulated teams and agencies
Accessibility and localization readiness
- Captions and transcripts available when required
- Localization-ready builds for multi-market rollouts when needed