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Laboratory Risk Assessment

A laboratory risk assessment should be performed periodically, such as annually, or when circumstances change like new equipment, procedures, or security threats. The risk assessment identifies hazards and risks, which are then used to implement controls and safety measures. Examples where a reassessment is needed include new infectious agents, equipment, personnel changes, or regulatory updates. Documentation of risk assessments allows for regular reviews of laboratory safety performance over time.

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393 views1 page

Laboratory Risk Assessment

A laboratory risk assessment should be performed periodically, such as annually, or when circumstances change like new equipment, procedures, or security threats. The risk assessment identifies hazards and risks, which are then used to implement controls and safety measures. Examples where a reassessment is needed include new infectious agents, equipment, personnel changes, or regulatory updates. Documentation of risk assessments allows for regular reviews of laboratory safety performance over time.

Uploaded by

Hawa
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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When to Perform and Review a Laboratory Risk Assessment

A periodic assessment of laboratory risk is important. When experiments, processes, and


technology change, so does the risk. A risk assessment should therefore be performed and
reviewed periodically - perhaps annually - although an organization should consider conducting
a risk assessment more often as circumstances warrant, for example, following the occurrence
of problems or if laboratory practices change.
Ideally, a laboratory should perform an initial risk assessment before any work is started. A risk
assessment should also be done whenever a change occurs. Examples of activities or events
that will change risk and warrant a reassessment include:
1. new infectious agents, toxins, reagents or other dangerous substances
2. new animal species, model, or route of administration of biological agents
3. new procedures and practices
4. new equipment
5. personnel changes
6. aging of equipment
7. advances in scientific understanding and technology
8. a recent or “near-miss” accident, theft, or security violation
9. national or regional changes in disease status
10. national, regional or local changes in threat environment or security environment
11. new local or national regulations
After reviewing the results of the risk assessment, measures should be made to amend or
update, as necessary. It is important to perform a risk assessment regularly or at a predefined
frequency.
Documentation is critical for future reviews when evaluating performance.

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