Industry leaders like Alcon, Johnson & Johnson MedTech, and Roche trust Planisware to manage complex portfolios, align investments, and ensure seamless collaboration across R&D, regulatory, and product development teams.
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Planisware is built for MedTech portfolio success
Developing medical technology means navigating multi-year product pipelines, evolving global regulations, and resource constraints that slow innovation. Planisware combines AI-driven forecasting, regulatory-first workflows, and deep portfolio visibility to align strategy with execution, eliminate bottlenecks, and bring products to market faster.
Purpose-built for MedTech teams
Developed with industry best practices and decades of expertise, Planisware delivers tailored workflows and risk management tools designed for medical technology development.
Integrated lifecycle management
Planisware unifies R&D, clinical, regulatory, and commercialization in one system to eliminate silos, ensure full traceability, and enable faster decisions.
AI-driven market acceleration
Predictive analytics and scenario modeling anticipate risks, optimize investments, and streamline approvals so you can bring your MedTech products to market faster.
Regulatory-first compliance management
Planisware automates compliance tracking for FDA, EU MDR, and ISO standards, integrating regulatory workflows to ensure audit readiness and speed up approvals.
Cross-functional integration
Planisware unifies ERP, PLM, QMS, CTMS, and regulatory databases in a single platform to eliminate data silos and enable real-time decision-making across teams.
Key software capabilities and features
Planisware gives world-leading MedTech teams the visibility, control, and agility to manage complex product development, navigate regulatory requirements, and accelerate time-to-market.
From built-in workflows for approvals to AI-driven PSO for resource management, Planisware’s industry-tailored PPM capabilities help you bypass bottlenecks and drive innovation across your medical technology portfolios.
Automate compliance & approvals
Reduce regulatory bottlenecks with audit-ready documentation and built-in workflows that accelerate approvals and keep life-saving treatments on track.
Increase portfolio visibility
Gain a single source of truth for multi-year product pipelines, regulatory milestones, and investment planning—ensuring alignment across teams and better decisions that speed up market delivery.
Maximize financial impact
Align R&D and CAPEX with strategic priorities, optimize budgets, and forecast funding to ensure innovation, evolution, and sustainment investments drive profitability and long-term growth.
Optimize resources and balance portfolios
Use AI-driven particle swarm optimization (PSO) to allocate talent, level workloads, and manage risk—ensuring a profitable mix of innovations and faster development.
Foster ideation & drive innovation
Empower teams to capture, evaluate, and advance top ideas through collaborative campaigns and scorecards—accelerating development and improving market entry with data-driven insights.
Turn MedTech challenges into opportunities
Discover how industry leaders optimize resources, accelerate innovation, and streamline compliance
MedTech leaders leverage Planisware’s advanced portfolio management tools to speed product development, optimize resources, and ensure compliance in a highly regulated industry.
Discover our 5-part MedTech miniseries
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Book a software demo
Learn how Planisware's tailored solutions can drive efficiency, compliance, and innovation in your medical technology projects and portfolios.