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This document provides guidelines for the safe transport of infectious substances and diagnostic specimens, applicable both nationally and internationally, emphasizing packaging, labelling, and documentation
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Organizations seeking approval or clearance for health-related products.
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Requirements for packagings of Category A infectious substances are found in §173.196, and must: meet the test standards of §178.609. be a triple packaging consisting of: - primary leakproof receptacle, - leakproof secondary packaging, and - rigid outer packaging.
Infectious substances that can cause disease in humans or both humans and animals are assigned to UN2814. For UN2900, infectious substances can cause disease in animals. UN2814 substances pose a high risk and require strict adherence to packaging, labeling, and documentation regulations.
Category A infectious substances must be tripled packaged and compliant with IATA Packing Instruction 602 diagrammed below.
Primary packaging is the packaging that comes into direct contact with your product, while secondary and tertiary packaging hold multiple units of your product. Each of these packaging types are made up different materials and are seen by different people in the distribution chain.
The basic triple packaging system: This packaging system consists of three layers: the primary receptacle, the secondary packaging and the outer packaging. The primary receptacle containing the specimen must be watertight, leak-proof and appropriately labelled as to content.
Category A infectious substances have two shipping names: “Infectious substances, affecting humans” (UN 2814) or “Infectious substances, affecting animals” (UN 2900). Category A infectious substances must be tripled packaged and compliant with IATA Packing Instruction 602 diagrammed below.
Requirements for infectious substances Infectious substances may only be transported in packaging which meets the UN class 6.2 specifications and packaging instruction (PI)602. This ensures that strict performance tests which include a nine metre drop test and a puncture test have been met.

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WHO/EMC/97.3 is a reporting framework established by the World Health Organization for monitoring and managing events related to public health emergencies.
Organizations and countries that are involved in public health response activities, particularly those responding to outbreaks or health emergencies, are required to file WHO/EMC/97.3.
To fill out WHO/EMC/97.3, the required fields should be completed accurately based on observed data, following the provided guidelines from WHO for the specific health event being reported.
The purpose of WHO/EMC/97.3 is to facilitate the collection of data related to public health emergencies to enable effective response, coordination, and resource allocation by health authorities worldwide.
Information that must be reported includes details about the health event, such as the type of emergency, number of cases, causal agents, and responses undertaken by health authorities.
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