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4.1 KiB
4.1 KiB
title, author, date, version, status
| title | author | date | version | status |
|---|---|---|---|---|
| Standard Operating Procedure for Handling Broken EEG Nets | 2026-01-05 | 1.0 | Draft |
1. Purpose
- Define standardized procedures for identifying, handling, documenting, repairing, or disposing of broken EEG nets.
- Ensure compliance with FDA 21 CFR Part 11, ISO 9001, and ISO 13485 requirements.
- Minimize risk to subjects, staff, and data integrity.
2. Scope
- Applies to all EEG nets used in clinical, research, or manufacturing environments within the organization.
- Covers detection of damage, removal from service, evaluation, repair, disposal, and documentation.
3. Definitions
- EEG Net: A multi-electrode sensor array used for electroencephalography data collection.
- Broken EEG Net: Any EEG net exhibiting physical damage, electrical malfunction, missing components, or performance deviation.
- Nonconformance: Failure to meet specified requirements.
4. Regulatory and Quality References
- FDA 21 CFR Part 11 – Electronic Records; Electronic Signatures
- ISO 9001 – Quality Management Systems
- ISO 13485 – Medical Devices Quality Management Systems
- Internal Quality Manual ""
- Risk Management Procedure ""
5. Responsibilities
- EEG Technician
- Identify and report broken EEG nets.
- Remove affected nets from service immediately.
- Quality Assurance (QA)
- Review documentation and assess compliance.
- Approve repair or disposal decisions.
- Engineering / Maintenance
- Evaluate damage and perform authorized repairs.
- Document Control
- Maintain records in accordance with Part 11 requirements.
6. Required Materials and Records
- Nonconformance Report (NCR) Form ""
- Equipment Log ""
- Repair and Maintenance Record ""
- Labeling materials for status identification
7. Procedure
7.1 Identification of Broken EEG Nets
- Inspect EEG nets before and after each use.
- Indicators of breakage include:
- Visible tears or frayed wiring
- Missing or damaged electrodes
- Signal noise or failure during testing
- Document findings immediately upon detection.
7.2 Removal from Service
- Tag the EEG net as "Out of Service".
- Remove from clinical or research area.
- Update the Equipment Log with date and reason.
7.3 Documentation
- Complete a Nonconformance Report with:
- Net identification number ""
- Description of damage ""
- Date identified ""
- Reporter name ""
- Ensure electronic records comply with 21 CFR Part 11 controls.
7.4 Evaluation and Disposition
- QA and Engineering assess:
- Severity of damage
- Impact on data integrity and safety
- Determine disposition:
- Repair
- Return to vendor
- Disposal
- Record justification for the decision.
7.5 Repair Process
- Perform repairs only by trained and authorized personnel.
- Verify functionality post-repair using approved testing methods.
- Document all repair activities and results.
7.6 Disposal
- Dispose of irreparable EEG nets according to waste management and environmental procedures.
- Remove asset from inventory records.
7.7 Return to Service
- QA approval required prior to reuse.
- Update status label to "Approved for Use".
- Archive all related records.
8. Training Requirements
- Personnel must be trained on this SOP prior to handling EEG nets.
- Training records shall be maintained and reviewed periodically.
9. Risk Management
- Identify risks associated with use of damaged EEG nets.
- Implement controls to prevent recurrence.
- Link nonconformance data to corrective and preventive action processes.
10. Deviations and Corrective Actions
- Document any deviations from this SOP.
- Initiate CAPA when trends or repeated failures are identified.
11. Records Retention
- Retain records according to Records Retention Policy "".
- Ensure secure storage and controlled access.
12. Change Management
- Changes to this SOP require review and approval per Document Control procedures.
- Maintain revision history.
13. Version Control
VersionDateDescription of ChangeAuthor1.02026-01-05Initial draft""
14. Approval Signatures
NameTitleSignatureDate""""""""""""""""""""""""