current language
Singapore available in the following languages:
or select your TÜV Rheinland country website:

Certification According to EN ISO 13485

Certification According to EN ISO 13485

Validating Your Quality Management System

Certifications build trust – a crucial factor when it comes to medical devices. EN ISO 13485 is the international standard for quality management systems for medical devices. We examine your quality management practices for medical devices, focusing on design and development, production, customer service, and assembly. Benefit from the positive effects of a quality management system: lean processes, efficient work flows, and international recognition.

Benefits at a Glance

EN ISO 13485 certification by the experts at TÜV Rheinland allows you to:

  • Communicate your high standards of quality
  • Gain a competitive edge thanks to independent certification
  • Use our accreditation as a notified body for all your medical devices
  • Benefit from our wealth of international experience in the medical devices market

Our Service to You:

  • EN ISO 13485 certification for your quality management system
  • EN ISO 13485 certification for processing of medical devices

MDSAP program covering the following regulations:

  • Australia: The Therapeutics Goods Administration – TGA
  • Brazil: The Brazilian National Health Surveillance Agency - ANVISA
  • Canada: Health Canada - CMDCAS
  • United States: U.S. Food and Drug Administration’s Center for Devices and Radiological Health
  • Japan: The Ministry of Health, Labour and Welfare (MHLW) and Pharmaceutical and Medical Devices Agency (PMDA)

Four Steps to Your Certificate

1. Optional Preliminary Audit
Preliminary assessment during which we inspect your site and review your quality management documentation.

2. Initial Certification Audit: Phase 1
We audit your site to determine whether you are eligible for certification or analyze all the required information on your company. We review your quality management documentation for compliance with EN ISO 13485.

3. Initial Certification Audit: Phase 2
On-site, we examine how your quality management system is applied in practice and evaluate how effective it is.

4. Certificate
If you meet all the criteria, we issue a certificate confirming compliance with standards and the integrity of your quality management system.

TÜV Rheinland: an Internationally Recognized Testing Body

EN ISO 13485 certification gives you advantages worldwide, not just on the European market. This certification is a prerequisite for marketing your products in other international markets.

Did you know? Neither a decision on granting certification nor any change of the certificate status (e.g. maintaining, renewing, refusing, suspending, restoring or withdrawing certification as well as expanding or reducing the scope of certification) is made by a single person! We always apply the four-eyes principle: The evaluation of the audit team /product expert is followed by a separate review and decision.

Offer

Any questions? Would you like an individual, non-binding offer? Then write to us now. We will respond to your request as quickly as possible.

pdf Questionnaire for the preparation of an offer for medical products 181 KB Download
pdf General Terms & Conditions 62 KB Download
pdf Testing & Certification Regulations 502 KB Download

Good Distribution Practice for Medical Devices (GDPMDS)

Good Distribution Practice for Medical Devices (GDPMDS) aimed to ensure that companies dealing with medical devices have a quality distribution system in place. Certification against GDPMDS ensures that products are consistently stored, transported, and handled under suitable condition as required by the marketing authorisation or product specification. Health Sciences Authority (HSA) has mandated the importers and wholesalers of medical devices in Singapore need to attain GDPMDS certification prior to the license application.

TÜV Rheinland is one of the accredited certification bodies identified by Health Sciences Authority (HSA) for GDPMDS certification. Alternatively, local manufacturers are exempted from certification to GDPMDS in their applications for importer's and/or wholesaler's licence(s), if the scope of their ISO 13485 certification covers storage and distribution of medical devices.

This might also interest you

Active Implantable Medical Devices (AIMD)

Active Implantable Medical Devices (AIMD)

Conformity Assessments for Your Active Implants.

more

Active and Non-Active Medical Devices

Active und Non-Active Medical Devices

Active and Non-Active Medical Devices.

more

In-vitro-Diagnostic (IVD)

In-vitro-Diagnostic (IVD)

We Can Test and Certify Your Quality Management System and Products.

more

International Approval for Medical Devices

International Approval for Medical Devices

Your Gateway to New Markets.

more

Medical Products (MDD)

Medical Products (MDD)

TÜV Rheinland offers a wide range of testing and certification services for Medical Devices

more

Tested Medical Device

Tested Medical Device

Market Your Products More Effectively with Voluntary Certification.

more

Contact

Get in contact with us!

Get in contact with us!

Last Visited Service Pages