Independent informational listing
Emergo by UL
Medical-device regulatory consulting and market-access provider with public services covering EU MDR, IVDR, quality systems and representation.
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Independent informational listing
RQM+
Medical-device and diagnostic regulatory and quality consulting organization supporting product development, submissions and lifecycle compliance.
COMPANY OVERVIEW
About RQM+
RQM+ presents a broad regulatory, quality and clinical consulting portfolio for medical devices and diagnostics. Its public services are relevant to manufacturers needing specialist support with EU MDR or IVDR strategy, technical documentation, quality systems, clinical or performance evidence and post-market obligations. Buyers should define the specific work packages, named experts, review responsibilities and acceptance criteria before the engagement begins.
Primary locationInternational provider with European teams
CoverageEurope and international markets
LanguagesEnglish and local-language availability varies by team
Evidence reviewed2026-08-28
Publicly described services
- EU MDR and IVDR consulting
- Regulatory submissions and strategy
- Quality-system support
- Clinical and performance evaluation support
- Post-market surveillance support
- Technical-documentation remediation
What to verify before appointment
Review the proposed experts' device experience, define document ownership and approval authority, and distinguish consulting from notified-body or authority decisions.
Official sources
SERVICES AND SCOPE
Services shown on this profile
- EU MDR and IVDR consulting
- Regulatory submissions and strategy
- Quality-system support
- Clinical and performance evaluation support
- Post-market surveillance support
- Technical-documentation remediation
COVERAGE
Where and how the provider works
Countries or regions
- Europe and international markets
Languages
- English and local-language availability varies by team
VERIFICATION REFERENCES
Evidence and public references
These references were supplied for the public profile. Confirm current validity, applicable scope and issuing-body status before relying on any claim.
Evidence last reviewed: August 28, 2026
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