Bureau Veritas is a global company with more than 80,000 employees worldwide. With our product testing, inspection and classification solutions, we make the world a safer place every day. Our
Accuprec is a Global service provider for various types of Regulatory testing services as well as Research based services required for Medical devices. Currently, we are working as an extended
bananaz is a cutting-edge AI-powered design management platform that helps modern engineering teams streamline collaboration, design change tracking, and validation in real time. Built for the
BEO BERLIN is your partner for an efficient conformity assessment procedure for medical devices. BEO BERLIN has been advising manufacturers on the testing and approval of medical devices for over 20
Redruth,
United Kingdom of Great Britain and Northern Ireland
Bluefruit Software has been providing high-quality embedded software solutions to clients worldwide for over 23 years. We have successfully delivered more than 100 embedded projects for clients in
Milton Keynes,
United Kingdom of Great Britain and Northern Ireland
BSI understands the challenges manufacturers face in bringing compliant products to market efficiently with absolute safety for patients. As a leading full scope EU Notified Body and UK Approved Body
We provide specialised certification, auditing and professional training services. Certiquality, acting as Notified Body (no. 0546) for Regulation (Eu) 2017/745, performs all evaluations required to
CETA Testsysteme GmbH Solution Partner for industrial Leak Testing and Flow Measurement CETA Testsysteme GmbH, based in Hilden near Düsseldorf, Germany, was founded in 1988 and has been active for
Delivering Solutions to the Medtech and Pharma Industry Clariscience provides Scientific Communication services and assistance to achieve Regulatory and Quality compliance. Consultancy is provided
MEDCERT is one of the largest certification bodies and Notified Bodies in Germany in the medical device industry. As a specialist for the certification of quality management systems and medical
Ente Certificazione Macchine is EU Notified Body No. 1282 for Medical Device Regulation (UE) 2017/745. With a twenty-year experience in the certification of products, machinery and work equipment,
Eurofins Biotech-Germande laboratory is specialised in supporting healthcare market key players in the hygiene and health sector. We perform wide ranges of standardised and customised tests and
Wolverhampton,
United Kingdom of Great Britain and Northern Ireland
Eurofins E&E offers a range of testing and certification services to help you get your medical devices to market on time and within budget. Our international network of accredited electrical and
We have combined our specific skills, gained through years of practical experience, to be able to offer effective solutions to the technical needs of those who, every day, choose us as their partner.
FIVE Validation offers GO!FIVE®, a SaaS-based validation solution designed to help companies meet EMA and FDA compliance up to 6 times faster than traditional paper-based or manual electronic methods
in.vent Clinical Services is a specialist department of in.vent Diagnostica GmbH, Europe’s leading experts for human biosample procurement. We assist our clients in the planning, setup, conduct
Time to market starts with trusted partnership and with more than 50 years experience Intertek developed partnering with global manufacturers to provide Medical Device assurance, testing, and
What is Biocompatibility? Biocompatibility is defined as the compatibility of materials, that are in physical, chemical or biological contact with the body, with the body’s systems, not