Product Intelligence for Bio & Medtech
As a bio or medtech company, you face unique challenges managing regulatory compliance, material traceability, and product data at scale. Dawn combines PLM, PDM, LCA, and data management in one platform, helping you manage ISO, CE, REACH, RoHS, and other certifications while linking compliance to cost forecasts and supplier data.
Maintain complete documentation, track materials and components with full traceability, and produce audit-ready data for regulatory submissions and customer requests.
Regulatory Compliance
Manage ISO, CE, REACH, RoHS, and other medical device certifications in one centralized library. Maintain complete documentation with version control and audit trails for regulatory submissions.
Material & Component Tracking
Track materials and components across your portfolio with complete traceability. Connect supplier data, risk signals, and cost forecasts to maintain audit-ready records.
Impact Assessments for Medical Devices
Conduct comprehensive LCAs for medical devices following ISO 14040/44 standards. Prepare EPD- and PEF-ready data linked to compliance and product documentation.
AI-Powered Efficiency
Accelerate compliance documentation and impact assessments with AI automation. Handle data import, CRUD updates, and preliminary assessments to reduce time-to-market.
Why Bio & Medtech Companies Choose Dawn
Manage regulatory compliance documentation in one centralized platform
Track materials and components with complete traceability for audits
Generate audit-ready impact data and compliance inputs
Accelerate product development with AI-powered automation
Meet customer requests for sustainability data and regulatory compliance
