Researchers and clinicians get faster access to critical evidence and AI-enabled answers they can trust.
Life science teams do not struggle because they lack data. They struggle because critical research and clinical and regulatory knowledge sit across disconnected systems, legacy repositories and spreadsheets. When that context is fragmented, AI doesn’t just slow teams down.
It produces results that are difficult to validate, explain or defend during regulatory review. Scientists spend more time hunting for and verifying evidence than focusing on science initiatives. AI helps this, but only when it is grounded in trusted scientific content with clear lineage and domain-specific meaning.
The Progress® Data Platform helps life science organizations connect scattered knowledge, apply shared context and put governed AI into real research and decision workflows, so evidence moves faster and defensibly.
"Developing a new drug takes over a decade and costs an average of $2.67 billion per asset."
Deloitte, Measuring the Return from Pharmaceutical Innovation, 2025
Proof That Science Teams Move Faster with Trusted Context
Success Story
Success Story
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You need faster access to prior findings, publications and internal know-how so teams spend more time on science and less on search.
You need clearer visibility across study documents, evidence and workflows without adding another disconnected system.
You need AI outputs that trace back to source evidence and stand up to regulatory review.
You need scalable data foundation that works with existing systems while improving meaning, reuse and control.
Helps researchers reach relevant evidence, prior experiments and supporting context faster, across disconnected repositories.
Connects structured and unstructured scientific content, adds shared meaning and grounds AI responses in authoritative sources.
Explore73% more correct answers and 41% reduction in poor-quality answers reported by pharma customer
Brings historical R&D into current workflows so teams build on what the organization already knows, instead of rediscovering it.
Makes archived content findable, reusable and interpretable across repositories and formats.
ExploreRWE catalog built in 6 months vs. industry average of 18+ months for comparable initiatives
Gives teams answers they can review, cite and defend in regulatory and clinical settings, not probabilistic guesses.
Preserves context, lineage and governance across research workflows so outputs stay tied to source material.
ExploreFortune 50 pharma replaced manual evidence catalog with governed, searchable RWE platform spanning millions of patient records
Connects research, quality and regulatory knowledge so teams act on the same trusted view, not competing versions of the truth.
Applies shared context across content and data so teams are not working from isolated versions of the truth.
ExploreFaster signal detection through semantic cross-source correlation vs. manual keyword review
Provides life science organizations a governed data foundation for AI, analytics and knowledge discovery. It connects enterprise data, applies shared context and governance and delivers trusted information into research, clinical and regulatory workflows, working alongside the systems teams depend on today.
Unifies clinical, research and regulatory data, regardless of format.
Understands scientific relationships between compounds, endpoints and regulatory concepts.
Enforces regulatory compliance, validation checks and audit trails.
Talk with a Progress specialist about the research, quality or regulatory decision you want to make faster, and defend with confidence.