Pharma / Biotech / Medical Devices

From Discovery to FDA Approval
In One Story

SlideStrike transforms your pipeline data into presentations that regulators, investors, and physicians actually understand. Your clinical results deserve better than PowerPoint from scratch.

🌐Available in 10 languages
0
Total Programs
$0M
Pipeline Value
0%
Avg Success Rate

R&D Pipeline Flow

276 programs → 6 NDA submissions. Your investors need to see why.

Discovery
2-3y
124
$580M
85%
-56 programs(45% attrition)
Preclinical
1-2y
68
$890M
72%
-26 programs(38% attrition)
Phase I
1-2y
42
$1240M
65%
-18 programs(43% attrition)
Phase II
2-3y
24
$2150M
48%
-12 programs(50% attrition)
Phase III
2-4y
12
$4280M
62%
-6 programs(50% attrition)
NDA/BLA
6-12m
6
$5670M
88%
High Success (≥70%)
Moderate (50-70%)
At Risk (<50%)
CRITICAL BOTTLENECK
Phase II Attrition
48% success rate
18 programs lost between Phase II and Phase III
STRONG PERFORMANCE
NDA/BLA Stage
88% success rate
6 programs with $5.7B combined value
EFFICIENCY METRIC
Discovery → NDA
4.8% success
6 of 124 programs reach NDA filing (industry: 5-10%)

Why Pharma/Biotech Teams Choose SlideStrike

Clinical data is complex. Your presentations don't have to be.

Pipeline Visualization

Auto-generate funnel charts, waterfall diagrams, and Gantt timelines from your pipeline data. Show investors exactly where value is created.

Clinical Trial Results

Kaplan-Meier curves, forest plots, safety summaries. Publication-quality charts in seconds, not hours with a biostatistician.

Multi-Audience Versions

One dataset → investor pitch, FDA deck, physician detail aid, patient brochure. All consistent. All compliant.

Regulatory-Ready

MLR-friendly language. Fair balance reminders. Citation management. Built for FDA advisory committees and EMA submissions.

Science-to-Story

AI translates p-values and hazard ratios into narratives that non-scientists understand. Keep the rigor, lose the jargon.

Data Integrity

AI validates numerical consistency across all slides. Never worry about a transcription error in front of the FDA again.

Generate Any Deliverable

From discovery updates to FDA submissions.

FDA Advisory Committee Presentations
Investor & Board Pipeline Updates
Clinical Trial Result Summaries
Medical Conference Posters
Mechanism of Action Explainers
Physician/KOL Detail Aids
Payer Value Dossiers
Patient Education Materials
R&D Portfolio Reviews
Patent Strategy Presentations
Partnership Pitch Decks
Regulatory Submission Support

The Communication Challenges You Know Too Well

The Translation Gap

Your Phase 3 data is groundbreaking. But the board doesn't speak p-values. Hours lost translating for non-scientists who control the budget.

The FDA Deck Pressure

One advisory committee meeting. 200 slides. A $2B drug approval on the line. No room for ambiguity, no tolerance for confusion.

The Audience Paradox

Same data, five different audiences: physicians, payers, investors, regulators, patients. Five different decks. Five different deadlines.

The Visualization Nightmare

Kaplan-Meier curves, forest plots, mechanism of action diagrams. Complex science that needs to be instantly understandable.

"We had 48 hours to prepare for an FDA advisory committee meeting. SlideStrike helped us generate 5 audience versions from the same clinical dataset. The committee chair said it was the clearest presentation they'd seen all year."

VP Medical Affairs
Mid-size Biotech

Tell Your Science Story

Communicate clinical data with the clarity and impact it deserves. From pipeline reviews to FDA submissions.