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IEC 62353 Recurrent Test Service (In-Service Testing) in Liberia
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IEC 62353 Recurrent Test Service (In-Service Testing) High-standard technical execution following OEM protocols and local regulatory frameworks.
Ensuring Patient Safety with IEC 62353 Recurrent Testing
Our IEC 62353 recurrent testing service in Liberia provides rigorous in-service electrical safety testing for medical devices. This ensures that equipment consistently meets international safety standards, safeguarding patient well-being and preventing electrical hazards within healthcare facilities.
Proactive Maintenance and Compliance for Medical Equipment
Beyond routine maintenance, our IEC 62353 testing offers a proactive approach to the ongoing electrical safety of medical devices in Liberian healthcare. By identifying and rectifying potential issues before they escalate, we minimize downtime, reduce repair costs, and guarantee continuous regulatory compliance.
Reliable Electrical Safety Assurance for Liberian Healthcare Providers
We offer a specialized IEC 62353 recurrent test service designed to provide Liberian hospitals, clinics, and medical centers with the highest level of assurance regarding the electrical safety of their medical equipment. Our certified technicians deliver accurate, documented testing to enhance operational reliability and uphold patient care standards.
What Is Iec 62353 Recurrent Test Service (In-service Testing) In Liberia?
IEC 62353, titled "Medical electrical equipment - Medical equipment in service - Routine inspection and test, maintenance and measuring", establishes a framework for the in-service testing of medical electrical equipment. This standard aims to ensure the continued safety and performance of medical devices once they are deployed in clinical environments, a process commonly referred to as "recurrent test service" or "in-service testing". In Liberia, as globally, adherence to IEC 62353 is crucial for maintaining patient safety, protecting healthcare professionals, and ensuring the reliable operation of medical infrastructure. The service involves a systematic process of inspections, functional tests, and performance measurements conducted at regular intervals throughout the lifecycle of a medical device. The primary objective is to identify and rectify potential hazards that may arise from wear and tear, damage, or environmental factors, thereby preventing equipment failure or malfunction that could compromise patient care or lead to adverse events.
| Service Component | Description | Objective |
|---|---|---|
| Visual Inspection | Comprehensive examination of the equipment's physical condition, including casing, connectors, cables, and accessories, for signs of damage, wear, or contamination. | To detect obvious physical defects that could compromise safety or functionality. |
| Protective Earth Continuity Test | Measurement of the resistance of the protective earth (ground) connection to ensure it is within acceptable limits, verifying the integrity of the safety earth path. | To confirm the effectiveness of the protective earthing system in preventing electric shock. |
| Insulation Resistance Test | Measurement of the resistance between electrical conductors and between conductors and accessible conductive parts to ensure adequate electrical isolation. | To verify that there are no unintended electrical leakage paths to the patient or operator. |
| Touch Current Measurement (Patient, Enclosure, Earth) | Measurement of the electrical current that could flow through a person in contact with accessible conductive parts of the medical device under normal and single-fault conditions. | To ensure that touch currents remain below established safety limits for patient and operator protection. |
| Functional Testing | Verification of the proper operation of all critical functions, controls, indicators, and safety mechanisms of the medical device. | To confirm that the equipment performs its intended medical function safely and reliably. |
| Performance Verification | Assessment of key performance parameters against the manufacturer's specifications, which may involve calibration checks or output measurements. | To ensure the accuracy and efficacy of the medical device's diagnostic or therapeutic output. |
| Documentation Review | Examination of maintenance logs, service records, and previous test results. | To establish a historical record of the equipment's maintenance and safety status, and to inform current testing. |
| Record Keeping and Reporting | Detailed documentation of all tests performed, results obtained, and any corrective actions taken, along with a certificate of compliance. | To provide a traceable record of the equipment's safety and maintenance status for regulatory, administrative, and liability purposes. |
Who Needs IEC 62353 Recurrent Test Service in Liberia?
- Healthcare Facilities: Hospitals, clinics, diagnostic centers, and other medical institutions utilizing medical electrical equipment.
- Manufacturers & Distributors: Companies that provide and service medical equipment within Liberia, often as part of their after-sales support and warranty obligations.
- Regulatory Bodies: While not directly performing the tests, governmental and quasi-governmental agencies responsible for healthcare quality and safety oversight may mandate or promote compliance.
- Third-Party Service Providers: Specialized biomedical engineering companies or independent service organizations offering equipment maintenance and testing services.
- Equipment Owners/Operators: Any entity or individual responsible for the safe operation and maintenance of medical electrical equipment.
Who Needs Iec 62353 Recurrent Test Service (In-service Testing) In Liberia?
IEC 62353, also known as "Medical electrical equipment - Routine checks and measurements after repair of medical electrical equipment," is a critical international standard for ensuring the safety and proper functioning of medical devices while they are in service. In Liberia, organizations and departments responsible for healthcare delivery and the management of medical equipment are the primary beneficiaries and users of IEC 62353 recurrent test services. This ensures that vital medical equipment remains safe for patients and operators, preventing potential harm and maintaining the quality of healthcare provided.
| Target Customer/Department | Specific Needs and Responsibilities related to IEC 62353 |
|---|---|
| Hospitals (Public and Private) | Biomedical Engineering Department: Responsible for the maintenance, repair, and safety testing of all medical equipment. They would directly commission and manage recurrent testing. Quality Assurance/Patient Safety Department: Oversees the overall safety of patient care, including the integrity of medical equipment. They would mandate and monitor compliance with standards like IEC 62353. Clinical Departments (e.g., Surgery, ICU, Radiology): Rely on functional and safe equipment for patient treatment. They are the end-users and are impacted by equipment failures or safety issues. |
| Clinics and Health Centers | Medical Officer/In-Charge: Often responsible for the upkeep of a limited range of medical equipment. They need assurance of equipment safety for routine patient care. |
| Diagnostic Laboratories | Laboratory Technicians/Managers: Operate specialized diagnostic equipment that requires regular calibration and safety checks to ensure accurate results and prevent hazards. |
| Medical Training Institutions with practical facilities | Technical Staff/Faculty: Ensure the safety of equipment used by students during practical training sessions to prevent accidents and instill good practices. |
| Non-Governmental Organizations (NGOs) involved in healthcare provision | Program Managers/Logistics Officers: Responsible for the procurement, deployment, and maintenance of medical equipment in their project areas. They need to ensure the safety and functionality of donated or purchased equipment. |
| Government Health Agencies (e.g., Ministry of Health) | Directorates of Health Services/Medical Equipment Management Units: Responsible for setting standards, policies, and overseeing the provision of healthcare services nationwide. They would promote, regulate, and potentially facilitate IEC 62353 compliance across public health facilities. |
Target Customers for IEC 62353 Recurrent Test Service in Liberia:
- Hospitals (Public and Private)
- Clinics and Health Centers
- Diagnostic Laboratories
- Medical Training Institutions with practical facilities
- Non-Governmental Organizations (NGOs) involved in healthcare provision
- Government Health Agencies
Iec 62353 Recurrent Test Service (In-service Testing) Process In Liberia
This document outlines the typical workflow for providing IEC 62353 recurrent testing (also known as in-service testing) services in Liberia, from the initial client inquiry to the successful execution of the test and subsequent reporting. The process is designed to ensure compliance with the IEC 62353 standard for the safety of medical electrical equipment during its operational life.
| Stage | Description | Key Activities | Responsible Parties | Deliverables/Outcomes |
|---|---|---|---|---|
| The client expresses interest in IEC 62353 recurrent testing services for their medical electrical equipment. | Client contact, initial discussion of needs, identification of equipment to be tested, clarification of scope and objectives. | Client (Healthcare Facility/Medical Device Owner), Service Provider (Testing Company) | Understanding of client's requirements, preliminary assessment of scope. |
| Based on the initial consultation, the service provider prepares a detailed proposal and quotation. | Assessment of equipment quantity, complexity, and location; preparation of a formal quotation outlining services, costs, timeline, and terms and conditions; negotiation and finalization of a service agreement. | Service Provider, Client | Formal quotation, signed service agreement/contract. |
| Once the agreement is in place, the testing schedule is confirmed and the client prepares the site. | Coordination of testing dates and times, identification of available access to equipment, ensuring necessary power sources and operating conditions are met at the client's facility. | Service Provider, Client | Confirmed testing schedule, readiness of the testing environment. |
| The qualified technicians from the service provider visit the client's facility to conduct the IEC 62353 tests. | Visual inspection, protective earth resistance testing, enclosure leakage current testing, patient leakage current testing (type BF, CF), insulation resistance testing, functional tests, record-keeping of all test results. | Service Provider (Qualified Technicians) | Raw test data, initial observations on equipment condition. |
| The collected test data is analyzed to determine compliance with IEC 62353 standards. | Review and interpretation of test results, comparison against IEC 62353 limits, identification of any non-conformities, compilation of a comprehensive test report including equipment details, test procedures, results, and recommendations. | Service Provider (Engineers/Technicians) | Detailed IEC 62353 test report. |
| If non-conformities are identified, the client may need to undertake corrective actions, followed by re-testing. | Client identifies and implements repairs or adjustments to faulty equipment, Service Provider conducts re-testing of affected equipment to verify compliance. | Client, Service Provider | Confirmation of successful remediation, updated test results. |
| Upon successful completion of all tests and any required re-testing, the client receives final documentation. | Issuance of a certificate of compliance for each tested equipment, provision of the final, signed test report, archiving of records by the service provider. | Service Provider | Certificate of compliance, final test report, client satisfaction. |
Key Stages of the IEC 62353 Recurrent Test Service Workflow
- Inquiry and Initial Consultation
- Quotation and Agreement
- Scheduling and Site Preparation
- On-site Testing Execution
- Data Analysis and Reporting
- Remediation and Re-testing (if applicable)
- Final Documentation and Certification
Iec 62353 Recurrent Test Service (In-service Testing) Cost In Liberia
The cost of IEC 62353 recurrent testing (in-service testing) for medical electrical equipment in Liberia can vary significantly due to several factors. As Liberia's healthcare infrastructure is still developing, specialized testing services might be less readily available and thus command higher prices compared to more established markets. The pricing is typically determined on a per-device basis, with factors like device complexity, age, and the specific tests required playing a crucial role.
Key Pricing Factors:
- Device Complexity and Type: Simpler devices like basic patient monitors or infusion pumps will generally cost less to test than more complex equipment such as MRI machines, CT scanners, or ventilators. The number of electrical and mechanical components, the intricacy of their interaction, and the safety features involved directly impact testing time and expertise required.
- Number of Devices: Bulk testing often leads to a lower per-unit cost. Service providers may offer discounts for testing larger quantities of equipment within a single facility.
- Location and Accessibility: Testing at remote or hard-to-reach healthcare facilities might incur additional travel and logistical costs, which would be passed on to the client.
- Service Provider Expertise and Certification: The qualifications, experience, and certifications of the testing technicians and the company itself are paramount. Highly skilled and certified professionals or accredited testing laboratories will likely charge more.
- Urgency of Service: If the testing is required on an urgent basis, expedited service fees may apply.
- Calibration and Repair Services: Sometimes, the recurrent testing might identify minor calibration issues or the need for small repairs. If these are included or performed by the same service provider, the overall cost will increase.
- Reporting and Documentation: The level of detail and formality required in the test reports can influence the cost. Comprehensive reports with detailed findings and recommendations might be more expensive.
| Pricing Factor | Impact on Cost | Considerations in Liberia |
|---|---|---|
| Device Complexity | Higher complexity = Higher cost | Variability is high. Basic ward equipment will be much cheaper than specialized ICU units. |
| Quantity of Devices | Bulk testing = Lower per-unit cost | Hospitals with larger equipment inventories might negotiate better rates. |
| Technician Expertise & Certification | Certified/Experienced = Higher cost | Limited availability of certified technicians may drive up prices. Reliance on external or international expertise can be costly. |
| Location & Logistics | Remote/Inaccessible = Higher cost | Challenges in transportation and access to remote healthcare facilities will add to the expense. |
| Inclusion of Minor Repairs/Calibration | Inclusion = Higher overall cost | Service providers might bundle minor adjustments, which is beneficial but increases the immediate cost. |
| Reporting Standards | Detailed/Formal = Higher cost | For compliance purposes, detailed reports are essential, potentially impacting the service fee. |
Estimated Cost Ranges in Liberian Dollars (LRD) per Device (Illustrative)
- Basic Medical Devices (e.g., thermometers, blood pressure monitors, simple infusion pumps): LRD 1,500 - LRD 3,500 per device.
- Intermediate Medical Devices (e.g., patient monitors, ECG machines, defibrillators): LRD 3,000 - LRD 7,000 per device.
- Complex Medical Devices (e.g., ventilators, anesthesia machines, basic imaging equipment): LRD 6,000 - LRD 15,000+ per device.
- Highly Complex/Specialized Equipment (e.g., MRI, CT scanners, advanced surgical lasers): LRD 20,000+ per device (requires specialized technicians and potentially on-site calibration/testing by international partners).
Affordable Iec 62353 Recurrent Test Service (In-service Testing) Options
Ensuring medical devices are safe and compliant with IEC 62353 standards through recurrent testing (in-service testing) is crucial for patient safety and regulatory adherence. Finding affordable options for this essential service can be a challenge for healthcare facilities. This guide explores value bundles and cost-saving strategies for IEC 62353 recurrent testing services.
| Value Bundle/Strategy | Description | Cost-Saving Benefits | Best Suited For |
|---|---|---|---|
| Multi-Device/Department Bundles | Negotiating a package deal for testing a group of devices or all devices within a specific department. This often involves a single contract and scheduling for multiple items. | Volume discounts, reduced administrative overhead per device, streamlined scheduling, and potential for dedicated technician visits. | Hospitals, large clinics, or facilities with a significant number of medical devices requiring regular testing. |
| Annual/Multi-Year Service Contracts | Committing to a service provider for a set period (e.g., 1, 3, or 5 years). These contracts often include preferential rates and priority scheduling. | Lower per-test costs over the contract duration, budget predictability, guaranteed service availability, and often includes calibration reminders. | Facilities looking for long-term cost stability and guaranteed service provision. |
| Tiered Service Levels | Offering different levels of service based on your needs and budget. This might range from basic compliance testing to comprehensive testing with detailed reporting and equipment history tracking. | Pay only for the services you truly need, allowing for cost optimization based on device criticality and risk. | Facilities with varying risk profiles for their medical equipment or those managing tight budgets. |
| Off-Peak Scheduling | Scheduling testing during non-peak hours, such as evenings, weekends, or during scheduled downtimes. Service providers may offer reduced rates for these less in-demand slots. | Direct reduction in per-test or hourly rates. | Facilities with flexible operational schedules or those willing to accommodate off-hour testing. |
| In-House Training & Partial Testing | While full IEC 62353 testing requires specialized equipment and expertise, some facilities may opt for in-house training for basic visual inspections and record-keeping, outsourcing only the complex electrical safety tests. | Reduced reliance on external technicians for simpler tasks, potentially lowering overall service costs. Requires investment in training and basic equipment. | Larger facilities with dedicated biomedical engineering departments and a commitment to developing internal capabilities. |
| Integrated Preventive Maintenance Programs | Combining IEC 62353 recurrent testing with broader preventive maintenance schedules for medical equipment. This can lead to consolidated service visits and potential discounts. | Reduced travel costs for technicians, fewer disruptions to clinical operations, and a holistic approach to equipment management. | Facilities aiming for efficient asset management and operational continuity. |
| Competitive Bidding and RFPs | Actively seeking quotes from multiple service providers and issuing Request for Proposals (RFPs) to ensure you are getting the best market rates. | Drives competition and allows for negotiation of more favorable pricing and service terms. | All facilities looking to secure competitive pricing. |
| Utilizing Vendor-Specific or OEM Services (with caution) | Original Equipment Manufacturers (OEMs) or their authorized service partners often have deep knowledge of their equipment. Sometimes, bundling testing with other OEM services can be cost-effective. | Potentially lower costs when bundled with other OEM services, but requires careful comparison with independent service providers. | Facilities that prioritize OEM expertise and have strong relationships with their equipment manufacturers. |
Understanding IEC 62353 Recurrent Testing
- IEC 62353, also known as 'Medical electrical equipment – Tests after repair and routine tests', specifies the procedures for testing medical electrical equipment to ensure its safety after repair or during routine in-service checks.
- Recurrent testing is essential to identify potential safety hazards that may have developed over time due to wear and tear, damage, or environmental factors.
- Key tests include visual inspection, protective earthing, insulation resistance, touch current, and functional tests.
- Regular testing helps prevent patient and operator harm, reduces the risk of equipment malfunction, and ensures compliance with regulatory requirements.
- The frequency of recurrent testing is determined by the device's risk classification, manufacturer recommendations, and local regulations.
Verified Providers In Liberia
In Liberia's evolving healthcare landscape, identifying trustworthy and competent healthcare providers is paramount for individuals and organizations seeking reliable services. Franance Health stands out as a leading example of a verified provider, distinguished by its commitment to rigorous credentialing, ethical practices, and a patient-centric approach. This document outlines Franance Health's credentials and articulates why they represent the best choice for healthcare needs in Liberia.
| Credential Type | Verification Source/Standard | Benefit to Patients |
|---|---|---|
| Ministry of Health Licensing | Liberian Ministry of Health | Ensures legal operation and adherence to national healthcare standards. |
| Professional Licenses | Issuing Medical Boards/Councils | Confirms qualifications and competence of individual medical practitioners. |
| International Accreditation (e.g., JCI, ISO - if applicable) | Accreditation Bodies (e.g., Joint Commission International, ISO Certification Bodies) | Demonstrates adherence to world-class quality, safety, and patient care standards. |
| Continuing Professional Development (CPD) | Internal training programs & recognized external courses | Guarantees that medical staff are up-to-date with the latest medical knowledge and techniques. |
| Data Privacy & Security Policies | National data protection laws & international best practices | Protects sensitive patient information and ensures confidentiality. |
| Ethical Conduct Guidelines | Professional medical ethics codes & organizational policies | Ensures fair, respectful, and patient-centered care. |
Franance Health's Key Credentials & Why They Matter
- {"title":"Accreditation & Regulatory Compliance","description":"Franance Health adheres to all national health regulations and standards set forth by the Liberian Ministry of Health. Furthermore, they are actively pursuing or have achieved relevant international accreditations (if applicable), demonstrating a commitment to global best practices in healthcare delivery and quality management. This ensures that all services provided meet stringent safety and efficacy benchmarks."}
- {"title":"Highly Qualified Medical Professionals","description":"The organization employs a team of licensed and experienced doctors, nurses, specialists, and allied health professionals. Each practitioner undergoes a thorough vetting process, verifying their educational qualifications, professional licenses, and clinical experience. Continuous professional development is a core value, ensuring staff remain up-to-date with the latest medical advancements and treatment protocols."}
- {"title":"Robust Patient Safety Protocols","description":"Franance Health has implemented comprehensive patient safety protocols, including infection control measures, medication safety procedures, and a commitment to patient privacy and data security. These protocols are designed to minimize risks and ensure a safe and secure environment for all patients."}
- {"title":"Commitment to Ethical Practice & Transparency","description":"The organization operates with a strong ethical framework, prioritizing patient well-being, informed consent, and equitable access to care. Transparency in billing, treatment options, and potential risks is a cornerstone of their patient interactions, fostering trust and empowering patients in their healthcare decisions."}
- {"title":"Advanced Facilities & Equipment","description":"Franance Health invests in modern medical facilities and equipment, enabling accurate diagnostics and effective treatments. The availability of advanced technology, coupled with skilled personnel, allows for a broader range of services and improved patient outcomes."}
- {"title":"Community Engagement & Public Health Initiatives","description":"Beyond direct patient care, Franance Health is actively involved in community health initiatives, health education programs, and preventive care campaigns. This demonstrates a broader commitment to improving the overall health and well-being of the Liberian population."}
Scope Of Work For Iec 62353 Recurrent Test Service (In-service Testing)
This Scope of Work (SOW) outlines the requirements for providing recurrent (in-service) testing services for medical electrical equipment according to the IEC 62353 standard. The objective is to ensure the continued safety and performance of medical devices while in active use. This SOW details the technical deliverables, standard specifications, and responsibilities of the service provider.
| Section | Description | Standard Specification | |||||
|---|---|---|---|---|---|---|---|
| 1.0 Scope of Service | Recurrent (in-service) testing of specified medical electrical equipment to ensure ongoing safety and performance. | IEC 62353:2014 (Medical electrical equipment - In-service inspection and testing after repair and routine testing) | |||||
| 2.0 Equipment to be Tested | Detailed list of medical electrical equipment requiring recurrent testing, including make, model, serial number, and location. (Refer to Appendix A for specific equipment list). | IEC 62353:2014, Clause 4.1 (General) | |||||
| 3.0 Testing Procedures | Conduct a comprehensive series of tests as defined by IEC 62353. This includes, but is not limited to: | IEC 62353:2014, Clause 4.2 (Routine Testing) | |||||
| 3.1 Visual Inspection | Thorough visual examination of the equipment for any physical damage, wear and tear, missing parts, and legible labeling. | IEC 62353:2014, Clause 4.2.1 | |||||
| 3.2 Protective Earth Resistance | Measurement of the protective earth conductor resistance to ensure effective earthing. | IEC 62353:2014, Clause 4.2.2.1 | |||||
| 3.3 Enclosure Leakage Current | Measurement of leakage current between accessible conductive parts and earth. | IEC 62353:2014, Clause 4.2.2.2 | |||||
| 3.4 Patient Leakage Current (Type BF, CF) | Measurement of leakage current from applied parts to earth for Type BF and CF applied parts. | IEC 62353:2014, Clause 4.2.2.3 | |||||
| 3.5 Patient Auxiliary Current | Measurement of leakage current in the patient connection circuit. | IEC 62353:2014, Clause 4.2.2.4 | |||||
| 3.6 Functionality and Performance Testing | Verification of essential functions and performance characteristics as per manufacturer’s specifications and intended use. | IEC 62353:2014, Clause 4.2.3 | |||||
| 4.0 Test Equipment | All testing shall be performed using calibrated and traceable test equipment meeting the requirements of IEC 62353. | IEC 62353:2014, Clause 4.3 | |||||
| 5.0 Acceptance Criteria | Equipment shall pass all tests as per the limits specified in IEC 62353 and relevant device-specific standards. | IEC 62353:2014, Clause 4.4 | |||||
| 6.0 Technical Deliverables | Upon completion of testing, the service provider shall deliver the following: | N/A | |||||
| 6.1 Test Report | A comprehensive report for each tested equipment item, including: | N/A | |||||
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| IEC 62353:2014, Clause 4.5.1 |
| 6.2 Test Labels | Affixing of a 'Tested' label on each piece of equipment indicating the date of testing and the next due date. | IEC 62353:2014, Clause 4.5.2 | |||||
| 6.3 Digital Records | Provision of digital copies of all test reports and associated documentation. | N/A | |||||
| 7.0 Service Provider Responsibilities | The service provider shall: | N/A | |||||
| 7.1 Employ qualified and trained technicians. | Maintain valid certifications for all test equipment. | Adhere to all safety protocols during testing. | Report any immediate safety concerns identified during testing. | Ensure minimal disruption to clinical operations. | Maintain confidentiality of all client information. | ||
| 8.0 Client Responsibilities | The client shall: | N/A | |||||
| 8.1 Provide access to equipment and testing locations. | Ensure equipment is available for testing during agreed-upon schedules. | Provide necessary power and environmental conditions for testing. | Inform service provider of any known issues or recent repairs to the equipment. | ||||
| 9.0 Schedule | Testing will be conducted on a recurrent basis (e.g., annually) as per the agreed schedule. (Refer to Appendix B for detailed schedule). | IEC 62353:2014, Clause 4.1 |
Key Objectives of Recurrent Testing
- Verify the continued compliance of medical electrical equipment with safety requirements after a period of use.
- Identify any degradation or faults that may have occurred during operation.
- Ensure the equipment performs its intended function safely.
- Minimize risks to patients and operators.
- Provide documented evidence of testing and compliance.
Service Level Agreement For Iec 62353 Recurrent Test Service (In-service Testing)
This Service Level Agreement (SLA) outlines the performance standards for the IEC 62353 Recurrent Test Service (In-Service Testing) provided by [Your Company Name]. It defines the guaranteed response times for incidents and the expected uptime for the service.
| Service Component | Response Time Guarantee (Business Hours) | Uptime Guarantee (Monthly) |
|---|---|---|
| Test Initiation Request Acknowledgement | 15 minutes | 99.5% |
| Critical Incident (Service Outage) | 1 hour | 99.9% |
| Non-Critical Incident (Functional Degradation) | 4 business hours | 99.5% |
| Reporting and Documentation Generation | 30 minutes (after test completion) | 99.8% |
| Data Retrieval Request | 2 business hours | 99.8% |
Service Components Covered
- Remote initiation of IEC 62353 recurrent tests on connected medical devices.
- Real-time monitoring and reporting of test results.
- Automated generation of test certificates and documentation.
- Secure storage and retrieval of historical test data.
- User authentication and access control for the testing platform.
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