Company Tagline
We don't make MedTech. We make MedTech happen.
Industry Category
Business Keywords
Company Description
RQM+ is a premier business consulting and services firm dedicated to accelerating the product lifecycle for MedTech innovations, from concept to patient impact. RQM+ applies end-to-end expertise to propel products through market entry and provide ongoing post-market support. The company offers tailored solutions that bring unmatched regulatory and quality expertise, FDA-recognized laboratory and materials science, comprehensive clinical trial design and execution, and impactful reimbursement strategies, accelerating market entry and commercial growth.
RQM+ partners closely with manufacturers across diverse device types and therapeutic areas to deliver life-changing technologies to patients faster, safer, and better. With a primary address at 2790 Mosside Blvd., Suite 800, Monroeville, PA 15146, US, and additional locations including Grosspeteranlage 29, Grosspeter Tower, Basel, 4052, CH, and 1 Ashley Road, 3rd Floor, Altrincham, Cheshire WA14 2DT, GB, RQM+ provides comprehensive support to its clients.
We invite the manager of RQM+ to create a customized and exclusive company showcase and product listing on our platform to further enhance RQM+'s market presence and connect with potential clients.
Key Personnel / Employees
Compare Companies Side by Side
Compare RQM+ with 3 companies in Business-Consulting-and-Services
| Comparison Field |
RQM+Main Company |
Fang ConsultingView Profile |
RegINTLView Profile |
Orca1.aiView Profile |
|---|---|---|---|---|
|
Founded Year
|
— | 1999 | 2023 | 2022 |
|
Company Size
|
— | 11-50 | 11-50 | 2-10 |
|
City
|
Monroeville, PA | Roseville, MN | Boston, MA | |
|
Country
|
United States | United States | ||
|
Skills & Keywords
Comparing with main company
|
25 Total Skills
MedTech CRO
Regulatory Consulting
Quality Assurance
Clinical Trial Design
Market Entry Strategy
Medical Device Manufacturing
Reimbursement Strategies
Manufacturing Site Transfer
Design History File Remediation
Human Factors
Design Verification & Validation
Regulatory for Medical Device
Complaint Remediation
Design Assurance for Medical Device
Quality Systems for Medical Device
Design Quality Assurance
510(k)
PMA
Remediation
Post-Market Surveillance for Medical Device
Clinical Evaluation Reports
De Novo
Product Quality for Medical Device
EU MDR
In Vitro Diagnostics
|
17 Total
1 Common
16 Unique
Match
4%
Common Skills:
Quality Assurance
Unique Skills:
21 CFR
CE Mark
Class I
Design Dossier Preparation
FDA
HIPAA Compliant
+10
|
9 Total
9 Unique
Unique Skills:
EMA
Global Regulatory Solutions
Medical Device Reporting
NDA/ANDA
OUS
Post Market Surveillance
+3
|
13 Total
13 Unique
Unique Skills:
AI
Data
EUA
FDA
FDA 483
HDE
+7
|
4
Total Companies1999
Oldest Founded1
Countries61
Unique SkillsSimilar Companies
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Alternative Company Names
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