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EUROPEAN STANDARDS PARTNER DIRECTORY

Find MDR and IVDR Consultants providers

Compare public profiles listed for MDR and IVDR Consultants, then open each company page to review services, coverage, evidence links and the applicable disclosure.

  • Clear company scope
  • Visible relationship disclosure
  • Public evidence references where supplied

PUBLIC COMPANY PROFILES

MDR and IVDR Consultants

5 profiles found

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Independent informational listing
MDR and IVDR Consultants

Emergo by UL

Medical-device regulatory consulting, in-country representation and human factors research for international market access.

  • Medical-device registration and regulatory strategy
  • EU MDR and IVDR support
  • Quality-management-system consulting

CoverageMedical-device market-access services across Europe and other international markets, confirm the relevant country team

Independent informational listing
MDR and IVDR Consultants

MDSS

Medical-device and IVD regulatory representation, registration support and regulatory training.

  • EU authorised representation
  • UK Responsible Person services
  • Swiss authorised representation

CoverageEU representation, with separate group services for the UK, Switzerland, USA, Australia and New Zealand

Independent informational listing
MDR and IVDR Consultants

NAMSA

Medical-device and IVD contract research, testing and regulatory consulting across product development and post-market work.

  • EU MDR and IVDR consulting
  • Clinical and performance evaluation support
  • Clinical and preclinical research

CoverageInternational medical-device and IVD projects, European locations include Belgium, France, Germany, Spain and the UK

Independent informational listing
MDR and IVDR Consultants

QbD Group

Life-sciences services covering regulatory affairs, quality assurance, validation, clinical work, laboratories and software.

  • MDR and IVDR regulatory support
  • Technical-documentation support
  • Quality assurance and audits

CoverageEuropean regulatory support with offices in Europe and Colombia, agree the project markets and delivery team

Independent informational listing
MDR and IVDR Consultants

RQM+

MedTech service provider offering regulatory and quality consulting, clinical trials, laboratory and materials work, and reimbursement support.

  • EU MDR and IVDR regulatory support
  • Quality-management systems
  • Clinical-trial services

CoverageUS, European and UK regulatory markets, confirm the specific engagement

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Directory disclosure

Profiles may be commercial partner profiles, disclosed platform relationships or independent informational listings. Inclusion does not create accreditation, certification, regulatory approval, exclusivity, editorial endorsement or a guarantee of suitability. Always verify current evidence and contractual scope directly with the provider and relevant issuing body.