Consulting and development services for MDR-compliant medical technology. Supports companies through regulatory strategy, risk management, quality optimization, and CE marking requirements to ensure patient safety and market compliance.
Manufactured by
3R LifeScience GmbH
Berlin, Germany
Product development and market approval of medical devices according to ISO 13485 and MDR 2017/745: Innovation management and development strategies Requirements management and integrated risk management Supplier management and outsourced processes External product development and project management Quality management processes and Technical Documentation Interim Management in regulatory affairs and compliance.
✦ Product-Specific Coverage
Based on AI-matched alternatives related to this product across Suplivia's medical sourcing network.
Generated for this product
AI-matched supplier coverage based on related product alternatives.
Corscience GmbH & Co. KG
Germany · 1 relevant product
Hangzhou Zhengda Medical CO.,Ltd
China · 1 relevant product
TS Quality & Engineering SRL
Italy · 2 relevant products
70 more relevant manufacturers available
Get free access to all relevant manufacturers for this product.
See all manufacturers →14 more sourcing countries available
Get free access to all sourcing countries identified for this product.
See all countries →See the full supplier coverage for this product
Get free access to all relevant manufacturers, sourcing countries, and product alternatives.
✓ Free for medical industry professionals.
from other manufacturers
from other manufacturers
3 of 112 closest product alternatives
Corscience GmbH & Co. KG · Germany
Engineering and regulatory consulting for safety-critical medical device development, including system architecture design, quality management, regulatory affairs support, and comprehensive testing and optimization services.
Hangzhou Zhengda Medical CO.,Ltd · China
Research and development services for medical device innovation and product development. Services support design, testing, and regulatory certification processes.
TS Quality & Engineering SRL · Italy
Comprehensive medical device consulting services covering design control, risk management, regulatory compliance (MDR, MDSAP), quality management systems (ISO 13485), and market introduction support. Services include mechanical design, FEA analysis, prototyping, DHF documentation, UDI implementation, and EUDAMED registration to facilitate product development from concept through global commercialization.
109 more product alternatives available
Create a free account to compare more product alternatives and supplier options.
© 2026 Suplivia · Home · Browse Products