Evidence OSMedical evidence & research
Pharma medical, R&D, and market access teams

Find the evidence your product actually lacks before deciding on the next research investment.

Organize work by product, indication, comparator, and development stage. Start with one evidence gap assessment, then choose a complete study or ongoing maintenance.

Illustrative scene: a health-product team reviewing products and documentation
Illustrative scene
Service usersR&D, medical affairs, clinical development, and market access teamsCommissioning partyThe pharmaceutical company or an explicitly authorized commissioning organization

Choose the deliverable you need

Inspect the value and deliverables, then agree scope, review and fees.

01 · FOCUSED

Research question & evidence gaps

Many studies exist, but a product question still has unresolved evidence gaps.

Core valueIdentify the evidence gaps that matter to one indication.
What you receiveDefine the population, intervention, comparator and unresolved outcomes.
  • PICO and research landscape
  • Key outcomes and evidence gaps
  • Recommended next scope

Study map and PDF; confirm the product question and purpose.

How fees workQuoted by product question and appraisal depth

Agree appraisal separately; execution modules are separate, with no duplicate charge for reusable work.

Scope limits

Excludes a full SR/Meta and trial execution.

02 · DEDICATED

Focused evidence work package

A development milestone needs evidence that can be reviewed and handed over.

Core valueDeliver a synthesis module the internal team can use.
What you receiveDeliver defined retrieval, appraisal or synthesis modules.
  • Search, screening and source index
  • Outcome evidence matrix and analysis figures
  • Methods review and handover guide

Report, CSV and agreed analysis attachments.

How fees workQuoted per retrieval, appraisal or synthesis module

Agree a fixed package by input volume, methods and professional review; milestone payments.

Scope limits

Excludes new indications and unagreed regulatory submissions.

03 · CUSTOM

Research & evidence maintenance

A long-running topic needs coordinated review and ongoing maintenance.

Core valueIdentify which product judgments new studies affect.
What you receiveMaintain defined questions and update the research baseline at agreed milestones.
  • Custom protocol and evidence baseline
  • Incremental appraisal and version register
  • Expert collaboration and staged delivery

Quote by milestones and cadence; no promise of regulatory or commercial outcomes.

How fees workBaseline work and maintenance quoted separately

Contract product, indication, questions and cadence; pay by milestones or maintenance period.

Scope limits

Excludes pharmacovigilance and statutory safety monitoring.

Amounts are proposed references or examples. Formal quotes depend on inputs, questions, professional review and acceptance scope. Agree updates separately; the same work is not charged twice.

What inputs are needed?
What stage is the product at?
Project initiation, clinical development, market access preparation, or post-market
Which claim needs support?
Target population, indication, comparator, and patient-important outcomes
Internal records and intended use
Trial data permissions, target markets, publication, and confidentiality boundaries
More situations

Situations and deliverables

NEXT STEP

Tell us the question. We’ll help define the scope.

Agree the scope, deliverables and review responsibilities before commissioning work.

Request scope & quote