From therapy validation to market access, every decision in healthcare carries real-world consequences. IDR connects organizations across the healthcare ecosystem with clinical and non-clinical experts. As a neutral partner, we don't shape the answers; we connect you with the experts who uncover them. We help the world's most ambitious healthcare organizations seize opportunities, avoid costly missteps, and, ultimately, save and extend lives.
Examples are illustrative, not exhaustive.
Validate scientific and commercial viability, assess competitive landscapes, and de-risk deals.
Identify viable drug targets, refine clinical trial design, and reduce time to market.
Engage former regulators and compliance experts to streamline approvals and reduce risk.
Understand payor expectations, pricing dynamics, and stakeholder perspectives by region.
Assess feasibility, efficacy, and strategic fit when entering new therapeutic areas, from tech to delivery.
Meet urgent due diligence needs by benchmarking emerging science, tech, and patient models against best-in-class players.
Expert Interviews:
Moderated, single- or double-blind sessions
Advisory Boards:
Curated panels for strategic input
Clinical Trial Support:
Insight on trial design, feasibility, and best practices
Regulatory Consulting:
Guidance on compliance, submissions, and policy shifts
Market Access Studies:
Pricing, payor, and procurement research across regions
Quantitative Research:
Survey data on behaviors, perceptions, and treatment trends
Dedicated project leads, 24/7 access, with support tailored to your brief. Each client gets a primary and secondary point of contact to ensure seamless coverage.
Our internal framework, aligned with ISO 27001, adapts to your needs. It supports industry-specific standards like GDPR and HIPAA, so you're protected at every step.