Aquí encontrará algunos documentos importantes para guiarlo en una solicitud de certificación de acuerdo con el nuevo Reglamento de Dispositivos Médicos y el Reglamento de Dispositivos Médicos de Diagnóstico In Vitro.


Centro de información de regulaciones de dispositivos médicos de la UE | SGS Argentina

Showcase Page

Office

Connectivity and Products

Health and Nutrition

Industries and Environment

Business Assurance

Natural Resources

Fax Number 1

Mechelen

Phone Number 1

Agricultural Commodities

Assessment Auditing and Certification

Automotive

Buildings and Infrastructures

Connectivity

Consulting Services

Cosmetics Hygiene

Digital Solutions for Connectivity and Products

Environment Health and Safety

Food

General Cybersecurity Services

Geochemistry

Government and Trade Facilitation

Hardgoods Toys and Juvenile Products

Health Science

Laboratory Testing Petroleum and Chemicals

Manufacturing and Processing Industries

Metallurgy and Consulting

Mineral and Metal Commodities

Mining Sites

OGC Commodities

Oil Gas

Power

Product Certification

Product Inspection

Softlines and Accessories

Supply Chain Assurance

Sustainability Assurance

Training

Transportation

BE SGS Belgium NV Mechelen 1

Services

EU Medical Devices Regulations Information Center

Centro de información de regulaciones de dispositivos médicos de la UE

Referencias

Contacta con nosotros

¿Qué estás buscando?

Algunos temas que podrían interesarte

Centro de información de regulaciones de dispositivos médicos de la UE

Referencias

Contacta con nosotros