Training and certification services for medical device manufacturers covering global regulatory standards, quality management systems (ISO 13485), and conformity assessment. Enables organizations to achieve compliance with international medical device regulations and obtain necessary notified body a...
Manufactured by
BSI Group Ltd.
Milton Keynes, United Kingdom
We guide you on your journey to meet global standards, promote safety, and enhance trust with your clients. As the world's first national standards body, our unrivalled global expertise and long-standing commitment to public benefit and innovation sets the benchmark for regulatory excellence. Our comprehensive portfolio offers you a wide range of proven regulatory and quality management services to support you in bringing compliant devices to market efficiently and safely. CE certification UKCA Certification ISO 13485 certification MDSAP Certification – Medical Device Single Audit Program and many more specialized solutions tailored to your regulatory needs.
✦ 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.
CERTEAFILES SAS
France · 1 relevant product
SigmaTech Nordic
Denmark · 4 relevant products
UL Solutions s.r.l.
Italy · 1 relevant product
80 more relevant manufacturers available
Get free access to all relevant manufacturers for this product.
See all manufacturers →13 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 115 closest product alternatives
CERTEAFILES SAS · France
Training and consulting services for medical device regulatory compliance, including technical documentation creation, MDR file management, and quality assurance strategies. Supports healthcare professionals in navigating EU 2017/745 regulations and preparing submissions for Notified Bodies.
SigmaTech Nordic · Denmark
QA training program supporting medical device companies in achieving CE marking compliance and ISO 13485 certification. Covers regulatory requirements, quality management systems, and documentation standards for diagnostic and therapeutic devices across European markets.
UL Solutions s.r.l. · Italy
Regulatory testing and certification services for medical devices, ensuring compliance with global safety and performance standards. Supports device manufacturers through independent assessment, documentation, and market authorization across multiple regulatory frameworks.
112 more product alternatives available
Create a free account to compare more product alternatives and supplier options.
© 2026 Suplivia · Home · Browse Products