Med-Di-Dia Limited Revenue
Medical Equipment Manufacturing • 
Galway, Co Galway, Ireland • 11-20 Employees
Med-Di-Dia Limited revenue & valuation
| Annual revenue | $1,026,660 |
| Revenue per employee | $86,000 |
| Estimated valuation?This valuation is estimated based on industry average for the Medical Equipment Manufacturing industry and current estimated revenues | $3,300,000 |
| Total funding | No funding |
Key Contacts at Med-Di-Dia Limited
Greer Deal
Director
Bobby Deal
Owner-Managing Director
Company overview
| Headquarters | Galway Technology Centre, Mervue Business Park, Galway, Galway H91 D932, IE |
| Phone number | +35391704804 |
| Websites | |
| NAICS | 3391 |
| Keywords | Risk Management, Quality Management, Quality Management Systems, Medical Devices, Cyber Security, Diagnostics, Artificial Intelligence, Technical Files, Regulatory Affairs, Cyber Security, Machine Learning, Digital Health, Iso 13485, Software Validation, Regulatory Strategy, Quality Compliance, Design Control, Product Classification, Iomt, Clinical Evaluations, Clinical Investigations, Eu Authorised Representative, Internet Of Medical Things, Samd, Corrective And Preventive Action (Capa), Design Files, Eu Legal Representative, Eu Person Responsible, Person Responsible For Regulatory Compliance, European Union Authorised Representative |
| Founded | 2019 |
| Employees | 11-20 |
| Socials |
Med-Di-Dia Limited Email Formats
Med-Di-Dia Limited uses 1 email format. The most common is {first initial} (e.g., j@med-di-dia.com), used 100% of the time.
| Format | Example | Percentage |
|---|---|---|
{first initial} | j@med-di-dia.com | 100% |
About Med-Di-Dia Limited
Med-Di-Dia, a regulatory affairs and quality compliance consultancy focusing on the Medical, Digital Health and Diagnostic sectors of the European Life Science Industry. With passion and drive, we have the flexibility to provide a cost-effective, bespoke solution that exactly fits the needs of you, the client. Time-critical services: - Person Responsible for Regulatory Compliance For micro and small companies, we will be your Person Responsible under the new EU Medical Device and In-Vitro Diagnostic Regulations. #PRRC - European Union Authorised Representative For non-EU and UK companies, we can be your Authorised Representative within Europe. #EUAR / #EAR - Legal Representative for EU Clinical Trials For organisations running EU-wide clinical trials, we will be happy to act as your Legal Representative to ensure continuity of your trials at a competitive price. Ongoing and routine services: - Help to define your product and develop your regulatory strategy. - Expertise to ensure a successful EU CE Mark registration. - Advice, guidance and implementation of all mandatory standards, such as ISO 13485:2016 (Quality Management Systems) Rest of World regulatory and quality compliance expertise is provided by our parent company, Global Regulatory Services (GRS) www.globalregulatoryservices.com
Employees by Management Level
Total employees: 11-20
Seniority
Employees
Employees by Department
Med-Di-Dia Limited has 1 employees across 1 departments.
Departments
Number of employees
Funding Data
Med-Di-Dia Limited has never raised funding before.
Med-Di-Dia Limited Tech Stack
Discover the technologies and tools that power Med-Di-Dia Limited's digital infrastructure, from frameworks to analytics platforms.
Widgets
Advertising
Web servers
Tag managers
Cookie compliance
JavaScript libraries
Miscellaneous
Programming languages
Miscellaneous
Security
Analytics
Cookie compliance
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