BIOMEDICAL ENGINEERING
- Medical Equipment Maintenance (PPM)
- Asset Replacement Program
- Staff Training
- Asset Audit and Condition Survey
- Medical Equipment Repairs
- Procurement Services
- Asset Management
Services
PROJECT MANAGEMENT
- Medical Device asset capture services
- Technical and financial audit services
- Device life-cycle management
- Risk Analysis
- Equipping solutions
- Facility upgrades
- Policy and procedure development and provision
- Cost reduction and recovery services
- Purchase and procurement support
ESTATES & FACILITY MANAGEMENT
Technical Support & Guidance
- Estates Management
- Medical Gases
- Staff Training
- Planned Preventative Maintenance Schemes
- Building Surveys
- Asset Management
- Regulatory Affairs
Medical Equipment Storage
The efficacy of Medical Equipment Libraries is well documented, and Key Health Solutions are well positioned to assist you with setting these up within your healthcare setting.
Our equipment management system has a specific Equipment Library module, enabling us to effectively manage all aspects of this service.
Medical Equipment Calibration
Key Health Solutions can provide on-site and off-site UKAS Accredited calibration services for Biomedical Engineering test equipment.
Our 24/7 customer support team are happy to help you from arranging a collection for your devices to delivery back to you.
Medical Equipment Audit Services
Key health Solutions have significant experience of
providing Technical and Quality Audit services, including
RFID asset labelling, to both the public and private sectors.
We provide these services to over 1500 healthcare establishments across the UK.
ISO CERTIFICATION Services For EBME Departments
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Environmental
- Ethical
- Equal Opportunities
- Training
- Data Protection and GDPR
- Mobile device
- Travel and Expenses
- Fire Safety
Subcontract Management
With our dedicated administration, engineering, and contract teams, we can assist you with effective management of specialist subcontractors.
We check all service reports to ensure all parts used and the works carried out, including full functional test, meet the specifications laid down by the OEMs and MHRA guidelines.
UK Responsible Person Services
Within the UK, all medical device companies must follow the Medicines & Healthcare products Regulatory Agency (MHRA) guidelines.
The MHRA guidelines specify that a UK Responsible Person (UKRP) must be appointed and must register the manufacturer, any relevant importers, and the devices with the MHRA.
Contact Us 24/7
Key Health Solutions, Shaftesbury Centre, Percy Street, Swindon, SN2 2AZ
