QA/RA Medical Device & IVD Consultancy UKRP - QMS - MDR - IVDR - ISO 13485 - CE Marking - Global Submissions - UKCA
IMed Consultancy Ltd is a leading medical device regulatory and quality consulting firm dedicated to guiding businesses through the complexities of global medical device regulations. With a focus on achieving compliance and fostering success, IMed Consultancy Ltd offers comprehensive support to companies of all sizes, from startups seeking initial guidance to large corporations requiring specialized project assistance or team training.
Located at Barford Road, Bloxham, England OX15 4FF, GB, IMed Consultancy Ltd prides itself on a team of industry experts who work closely with clients to achieve their goals, transfer knowledge, and ensure they reach their desired outcomes. The company’s flexible, friendly, and straightforward approach has enabled them to build long-standing relationships based on trust and an in-depth understanding of each client’s unique business needs.
IMed Consultancy Ltd specializes in global registrations, clinical evaluations, and navigating various regulatory pathways, including TGA, 21 CFR Part 820, and more. With expertise in ISO 13485, CE Marking, UKCA, and other critical standards, IMed Consultancy Ltd ensures that medical devices and in vitro diagnostics meet the highest quality and regulatory requirements. We invite the manager of IMed Consultancy Ltd to create a customized and exclusive company showcase and product listing on our platform to further enhance their market presence.
Compare IMed Consultancy Ltd with 3 companies in Medical-Equipment-Manufacturing
| Comparison Field |
IMed Consultancy LtdMain Company |
Johner Institut GmbHView Profile |
ApotechView Profile |
RemedicalView Profile |
|---|---|---|---|---|
|
Founded Year
|
— | 2005 | 2020 | 2022 |
|
Company Size
|
— | 51-200 | 11-50 | 2-10 |
|
City
|
Bloxham, England | Konstanz, Baden-Württemberg | London, England | |
|
Country
|
Germany | United Kingdom | ||
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Skills & Keywords
Comparing with main company
|
25 Total Skills
Medical Device Regulations
Quality Consulting
Global Registrations
ISO 13485
CE Marking
Regulatory Affairs
IVDR
Clinical Evaluations
TGA
21 CFR Part 820
Technical Files
IVD
510k
ISO 14971
Auditing
MDSAP
MDR
Risk Management
Health Canada
Medical Devices
In Vitro Diagnostics
QMS
FDA
UKCA
UK Responsible Person
|
18 Total
18 Unique
Unique Skills:
510(k)
Audit
Clinical Evaluation
Clinical Investigation
Elearning
Electrical Safety
+12
|
16 Total
16 Unique
Unique Skills:
Audit
Biotech
Commissioning & Qualification
Computer Systems Validation
EMA
GCP
+10
|
18 Total
18 Unique
Unique Skills:
Audit readiness
Automation
Complaint Handling
Compliance
Consulting
Design Control
+12
|
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