Transfer your medical device certification to DNV

Speak with our medical device team to discuss your current certification status and explore the next steps.

Journey continues on Veracity, DNV's trusted digital platform.

Transfer your medical device certification to DNV

Why transfer your certification to DNV?

Changing certification partners can help reduce delays, improve responsiveness and support ongoing compliance. We can review your existing MDR, IVDR, ISO 13485, MDSAP or other certification status and guide you through the next steps.

What you gain with DNV

Medical device expertise

Dedicated medical device assessors and auditors with experience across a broad range of technologies and risk classes.

Multiple certification pathways

Support your certification journey across MDR, IVDR, ISO 13485, TCP III and MDSAP.

Global reach, local support

Active in more than 100 countries with local teams supporting manufacturers worldwide.

Digital certification experience

Our secure digital platform provides access to certification documents and certification activities, helping improve transparency and efficiency throughout the certification process.

Independent and trusted assurance partner

More than 160 years of helping organizations build trust and demonstrate compliance.

Streamline certification across MDR, IVDR, MDSAP, TCP III and ISO 13485

Medical device certification transfer process

  1. Submit your enquiry: Provide information about your organisation, current certification status and areas of interest.
  2. Initial assessment and planning: Our team reviews your documentation and certification status, then works with you to understand your business objectives, timelines and regulatory needs. Together, we determine the most appropriate transfer pathway and certification strategy.
  1. Document transition: We examine your technical files and previous assessments.
  2. Conformity assessment: Our team performs the required reviews and audits.
  3. Certification: Once approved, you receive your certificate from DNV.  
Gloved clinician adjusting an intravenous infusion set, illustrating medical device safety checks, functional performance testing, and regulatory compliance.

Supporting your certification journey

Your certification partner should help you navigate regulatory requirements with confidence. Whether your needs have evolved, your organization is growing, or you are looking for a different level of support, we can assess your current certification status and help determine the best next steps.

Frequently asked questions (FAQ)

  • Transfer options vary depending on the certification scheme, certification status and applicable regulatory requirements. Our team can review your situation and discuss the available pathways.

  • You can use this form to enquire about MDR, IVDR, ISO 13485, MDSAP, Malaysia Medical Device Registration, TCP III and other medical device certification-related services.

  • Timeframes vary depending on the certification scheme, certification scope and current certification status. Our team can provide more information once we understand your requirements.

  • Depending on the certification schemes involved, opportunities may exist to coordinate certification activities. This can be discussed during the initial review process.

  • To assess the available transfer options, we typically require information about your organisation, current certification status, certification scope and the certification scheme involved (for example MDR, IVDR, ISO 13485 or MDSAP). Depending on the circumstances, we may also need information about your products, current certification body and certification timelines. Our team will guide you through any additional information required during the review process.

  • Yes. The form can be used for both transfer enquiries and organisations exploring certification for the first time.

Our certification services

MDR Certification | EU Notified Body #2460

Secure EU market access and navigate Medical Device Regulation (MDR) compliance with confidence through DNV’s expert certification services and global regulatory support.

Find out more about MDR certification

IVDR Certification | EU Notified Body #2460

Gain EU market access for your in vitro diagnostic devices with DNV, a designated Notified Body under the In Vitro Diagnostic Regulation (IVDR – EU 2017/746).

Find out more about MDR certification

MDSAP Certification

Streamline global market entry with DNV’s MDSAP certification. A single regulatory audit covering multiple jurisdictions helps medical device manufacturers achieve more efficient compliance across key markets.

Find out more about MDSAP certification

ISO 13485 Certification

Achieve global market access and regulatory compliance with confidence through DNV’s ISO 13485 certification services for medical device quality management systems. 

Find out more about ISO 13485 certification

TCP III Certification

Secure a stronger position in Taiwan’s medical device market with DNV’s TCP III Certification, enabling faster, cost-effective compliance through coordinated EU–Taiwan conformity assessments. 

Find out more about TCP III certification

Transfer your certification to DNV

We combine deep regulatory knowledge with industry-wide experience, enabling you to navigate complex requirements with clarity and confidence.

Switch your certification to DNV

Make the switch. Start your transfer today

Take the next step toward smoother certification. Contact DNV to begin the transfer process.