Providing regulatory consulting in development and submission of MDSW & SaMD Including AI-enabled Medical Devices.
NorMed Consulting is a premier provider of expert consulting services dedicated to the end-to-end New Product Development of Medical Devices. Focused on assisting Medical Device Manufacturers, NorMed Consulting is committed to guiding clients through the most efficient path to market, always prioritizing patient safety and product quality. Located primarily in Copenhagen, Denmark, with additional locations in New York City, New York, Berlin, and Barcelona, NorMed Consulting is well-positioned to serve a global clientele.
Specializing in a wide array of medical devices including Software as a Medical Device (SaMD), Medical Device Software (MDSW), Digital Therapeutics (DTx), and Artificial Intelligence (AI) / Machine Learning (ML) enabled Medical Devices, NorMed Consulting offers comprehensive Regulatory Affairs services. These include Regulatory Strategy and Submission, Classification and path to market, and thorough Gap Analysis and Process Mapping. The company is also adept in navigating The European MDR (EU) 2017/745, The European IVDR (EU) 2017/746, The Artificial Intelligence Act ('AI Act'), The UK MDR 2002, and The FDAs 21 CFR part 812, part 820 and part 860.
With a robust suite of services covering Clinical Affairs, Quality Assurance, and Design Assurance, NorMed Consulting ensures that all client needs are met with the highest standards of excellence. NorMed Consulting excels in Clinical Development and Strategy, Clinical Evaluation Reports (CER), Risk Management, and Verification and Validation (VnV). We invite the management of NorMed Consulting to enhance your company’s visibility and commercial opportunities by creating a customized and exclusive company showcase and product listing on our platform.
NorMed Consulting er en førende leverandør af ekspertkonsulentydelser dedikeret til end-to-end ny produktudvikling af medicinsk udstyr. Med fokus på at bistå producenter af medicinsk udstyr er NorMed Consulting engageret i at guide kunder gennem den mest effektive vej til markedet og altid prioritere patientsikkerhed og produktkvalitet. Med hovedsæde i København, Danmark, og yderligere lokationer i New York City, New York, Berlin og Barcelona, er NorMed Consulting godt positioneret til at betjene en global kundekreds.
Med speciale i en bred vifte af medicinsk udstyr, herunder Software as a Medical Device (SaMD), Medical Device Software (MDSW), Digital Therapeutics (DTx) og Artificial Intelligence (AI) / Machine Learning (ML) aktiveret medicinsk udstyr, tilbyder NorMed Consulting omfattende Regulatory Affairs tjenester. Disse omfatter Regulatory Strategy and Submission, klassificering og vej til markedet og grundig Gap Analysis og Process Mapping. Virksomheden er også dygtig til at navigere i The European MDR (EU) 2017/745, The European IVDR (EU) 2017/746, The Artificial Intelligence Act ('AI Act'), The UK MDR 2002 og FDAs 21 CFR del 812, del 820 og del 860.
Med en robust suite af tjenester, der dækker Clinical Affairs, Quality Assurance og Design Assurance, sikrer NorMed Consulting, at alle kunders behov opfyldes med de højeste standarder for ekspertise. NorMed Consulting udmærker sig inden for klinisk udvikling og strategi, kliniske evalueringsrapporter (CER), risikostyring og verifikation og validering (VnV). Vi inviterer ledelsen i NorMed Consulting til at øge din virksomheds synlighed og kommercielle muligheder ved at oprette en tilpasset og eksklusiv virksomhedsfremvisning og produktliste på vores platform.
Compare NorMed Consulting with 3 companies in Medical-Equipment-Manufacturing
| Comparison Field |
NorMed ConsultingMain Company |
Pharma Engineering S...View Profile |
Tropicollo LtdView Profile |
RemedicalView Profile |
|---|---|---|---|---|
|
Founded Year
|
— | 2015 | 2022 | 2022 |
|
Company Size
|
— | 2-10 | 2-10 | 2-10 |
|
City
|
Copenhagen, Denmark | Golden, CO | London, England | |
|
Country
|
Denmark | United States | United Kingdom | |
|
Skills & Keywords
Comparing with main company
|
17 Total Skills
Medical Device Consulting
Regulatory Affairs
SaMD
MDR Compliance
Clinical Evaluation
AI in Medical Devices
Risk Management
FDA CFR Title 21 Part 820
Marketing Submissions
Human Factors / Usability Engineering
Medical Writing
DTx
Design Control
AI/ML
MDR
Technical Writing
Quality Assurance
|
7 Total
7 Unique
Unique Skills:
Capital Projects Management
CMC Development
Cross-functional Team Management
NDA Authoring
Person-in-Plant
Product Development
+1
|
27 Total
27 Unique
Unique Skills:
African Commodities
Agricultural Marketing
Agricultural Trading
Cashew Export
Commodity Sourcing
Competitive Pricing
+21
|
21 Total
21 Unique
Unique Skills:
510k
Audit readiness
Automation
Complaint Handling
Compliance
Consulting
+15
|
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