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Animal Exposure Awareness Occupational Animal ExposureBoth research and nonresearch animals have the potential to cause injury, transmit zoonotic diseases, and/or cause allergic reaction to those
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Gather all necessary information including the type of animal exposure, details about the animal involved, and any symptoms experienced.
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Complete the appropriate sections on the Animal Exposure REM form including personal information, type of exposure, and any actions taken.
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Ensure all sections are filled out accurately and thoroughly to provide relevant information for healthcare professionals.

Who needs rem - animal exposure?

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Individuals who have been exposed to animals and may be at risk of developing infections or diseases from the exposure.
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Healthcare providers who need to assess and provide treatment for individuals who have had animal exposure.
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REMS stands for Risk Evaluation and Mitigation Strategy. REMS - Animal Exposure refers to reports of adverse events involving animal exposure to medications or products.
Manufacturers, distributors, and marketers of medications or products that may pose a risk of animal exposure are required to file REMS - Animal Exposure reports.
REMS - Animal Exposure reports can be filled out online through the FDA's electronic submission portal or by submitting a paper form to the FDA.
The purpose of REMS - Animal Exposure is to monitor and document any adverse events involving animal exposure to medications or products in order to protect animal welfare.
Information such as the type of medication or product, the nature of the animal exposure, any resulting adverse events, and any actions taken in response to the exposure must be reported on REMS - Animal Exposure.
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