Regulatory affairs leads at biotech and pharma teams
Need a piece that aligns with label language and fits inside dossier or briefing materials.
Use case
MOA video for regulatory materials
A clear visual MOA helps reviewers follow the science quickly. CDI Studio works alongside your scientific and regulatory leads on animations that ground each frame in peer-reviewed sources or PDB structures, with reference documentation that travels with the dossier. A practical fit for small and mid-size biotech, pharma, and drug-related teams preparing their next submission.
Cited
Per-scene reference documentation
Reviewable
Sponsor scientific review at every stage
Plain language
Reviewer-friendly visual narration
What we build
- Reference-documented MOA animations
- Submission-friendly stillframe galleries
- Section 14 and clinical study report visualizations
- Subgroup-analysis explainer animations
- Mechanism + dose-response combined videos
Who briefs us
CMOs preparing for review meetings
Want a visual that helps reviewers and committee members see what the drug does.
Medical writers
Want a complementary visual to an existing CSR or briefing document.
Common formats
Reference-grounded MOA
Standard 30 to 60 second piece with PDB and peer-reviewed citations documented.
Stillframe gallery
Eight to twelve high-resolution stills extracted from the animation for printed dossiers.
Review-meeting cut
Short muted loop suitable for in-meeting playback.
Frequently asked
Do you have experience with regulatory-supporting work?
Yes. Several CDI projects have been included in regulatory packages and review meeting decks. We document references at storyboard sign-off so they travel with your dossier.
What review process do you support?
We support sponsor scientific review at script and storyboard, and a final medical legal review cycle before delivery if your team needs it.
Ready to start?
Send us your science, target audience, and deadline. We will scope and price within 48 hours.