The Biological Risk Assessment Form is a critical document required under Nigerian biosafety regulations, particularly the National Biosafety Management Agency Act 2015 and National Biosafety Guidelines 2019. This document must be completed before commencing any work with biological materials or agents in research, healthcare, or industrial settings. It serves as both a legal requirement and a practical tool for identifying potential hazards, evaluating risks, and establishing appropriate control measures. The form is designed to protect workers, the environment, and the public by ensuring proper risk management practices are in place. It must be regularly reviewed and updated, especially when there are changes in procedures, personnel, or biological agents being used.
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1. 1. General Information: Basic details including facility name, location, department, assessment date, and assessor information
2. 2. Project/Process Description: Detailed description of the biological work/research being conducted, including scope and objectives
3. 3. Biological Agent Information: Specific details about the biological agents involved, including classification, risk group, and characteristics
4. 4. Laboratory/Facility Information: Description of the work area, containment level, and existing safety measures
5. 5. Risk Identification: Identification of potential hazards and routes of exposure
6. 6. Risk Analysis: Evaluation of likelihood and severity of identified risks
7. 7. Control Measures: Existing and proposed control measures, including engineering controls, PPE, and administrative controls
8. 8. Emergency Procedures: Specific procedures for handling accidents, spills, and exposures
9. 9. Training Requirements: Required training for personnel involved in the work
10. 10. Monitoring and Review: Procedures for monitoring control measures and reviewing the assessment
1. Environmental Impact Assessment: Required when the work may have environmental implications or involves GMOs
2. Transportation Procedures: Include when biological materials need to be transported between facilities
3. Animal Handling Procedures: Required when work involves animal specimens or testing
4. Decontamination Procedures: Detailed when specific decontamination protocols are needed beyond standard procedures
5. Community Impact Assessment: Required for high-risk activities that might affect surrounding communities
1. Appendix A: Risk Matrix: Standard risk assessment matrix for evaluating likelihood and severity
2. Appendix B: Biological Agent Classification Table: Reference table for biological agent risk groups and characteristics
3. Appendix C: PPE Requirements Chart: Detailed chart of required personal protective equipment for different activities
4. Appendix D: Emergency Contact Information: List of emergency contacts and response procedures
5. Appendix E: Incident Report Form: Template for reporting accidents, spills, or exposure incidents
6. Schedule 1: Safety Equipment Checklist: Checklist of required safety equipment and their maintenance schedule
7. Schedule 2: Training Record Template: Template for recording completed training requirements
Relevant legal definitions
Clauses
Relevant Industries
Healthcare
Research and Development
Pharmaceutical
Biotechnology
Agriculture
Education
Medical Laboratories
Food and Beverage
Environmental Services
Waste Management
Chemical Manufacturing
Relevant Teams
Research and Development
Quality Assurance
Environmental Health and Safety
Laboratory Operations
Compliance and Regulatory Affairs
Facilities Management
Clinical Operations
Biosafety Committee
Risk Management
Production
Relevant Roles
Laboratory Technician
Research Scientist
Biosafety Officer
Quality Assurance Manager
Environmental Health Officer
Laboratory Manager
Principal Investigator
Safety Coordinator
Microbiologist
Biotechnology Researcher
Clinical Laboratory Supervisor
Research Director
Compliance Officer
Facilities Manager
Laboratory Safety Specialist
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