SAMOCYBERSHIELDPROJECT-BASED · REMOTE COLLABORATION
Scoped support for medical technology and rehabilitation robotics teams, combining Information Engineering, clinical rehabilitation experience and hands-on medical-equipment service work.
Help organise product context, user needs supplied by the client, system boundaries, interfaces, assumptions and traceable requirements into reviewable working documents.
Possible outputs: requirements register, system overview, interface list, traceability table.Prepare or review system descriptions, component and interface notes, service procedures and technical reports using information and design decisions verified by the client’s responsible engineers.
Possible outputs: document set, service notes, configuration records, technical report.Structure preliminary verification plans, checklists, acceptance criteria drafts and evidence/report templates. Planning and documenting a test is distinct from performing, approving or certifying it.
Possible outputs: draft test protocol, checklist, results template, issue log.Help teams translate rehabilitation workflows and therapist or user observations into clear engineering questions, use scenarios and design inputs for review by the product team.
Possible outputs: workflow map, use-context summary, design-input discussion paper.Discuss service documentation and troubleshooting workflows informed by previous medical and physiotherapy equipment experience, within the equipment, information and authorisations available for the assignment.
Possible outputs: maintenance checklist, troubleshooting guide draft, service-record structure.Support remote review meetings, issue tracking and handover between clinical, engineering and service stakeholders for a clearly bounded work package.
Possible outputs: action log, decision record, handover summary.Turn client-defined clinical and engineering needs into vendor-neutral technical criteria, and structure comparisons of supplier offers against specifications, compatibility, service support and documentation supplied by the client.
The client retains supplier selection, commercial negotiation, purchase approval and ordering. Public-tender work is not offered as a standalone service.Email a short, non-confidential summary. Do not send patient data, passwords, proprietary files or sensitive information at first contact.
Agree what is in scope, which source information is authoritative, who reviews the work and what is explicitly excluded.
Before paid work, agree a written scope, responsibilities, schedule, fees, confidentiality and data-handling arrangements.
Deliver drafts or records for the client’s qualified team to review, approve and use within its own quality and regulatory processes.
Where relevant to the product, intended purpose and project stage, a team may need to consider ISO 13485 for medical-device quality management, ISO 14971 for risk management, and applicable IEC standards. For rehabilitation robots that physically interact with a patient, IEC 80601-2-78:2019+AMD1:2024 may be relevant to basic safety and essential performance. The applicable set must be determined for each project by the responsible manufacturer and qualified regulatory specialists.
Referencing a standard does not mean this service certifies compliance, performs an independent conformity assessment, approves a medical device, or replaces the client’s quality, regulatory, safety or legal responsibilities. Verification plans and reports must be reviewed and approved by the responsible project team.
This website does not offer patient-specific advice, clinical evaluation, certification, CE marking, notified-body services, formal regulatory submissions, or claims that SAMO Rehabilitation is a finished or tested robot.
Samuel Motlagh has a Bachelor’s degree in Information Engineering (L-8) from the University of Padova, a background in physiotherapy and osteopathy, and previous service-engineer experience with medical and physiotherapy equipment, including troubleshooting, calibration, repair and preventive maintenance.
Assignments are accepted only where the requested scope matches the available experience and can be responsibly bounded. Specialist PCB layout, firmware development, full product design, safety approval and formal regulatory assessment are not represented as services on this page.
Include the type of device or system, the specific support you are looking for, your expected deliverable and a rough timeline. Keep the first message non-confidential.
Samuel will review the request and, if it fits, discuss scope and written terms. The website itself does not take orders or payments.
NO ONLINE CHECKOUTScope and status
Independent, project-based professional enquiries are handled by Samuel Motlagh. SAMO CyberShield is the project/website name and is not presented here as a registered company. No medical-device certification, regulatory approval, completed SAMO robot, or clinical validation is claimed. Do not send health or other sensitive data by email.