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Where is information on storage requirements for the investigational product usually found?

  1. On the product code-breaker label

  2. In the CRF directions

  3. In the drug accountability log

  4. In the study protocol

The correct answer is: In the study protocol

Information on storage requirements for the investigational product is usually found in the study protocol. The product code-breaker label is a physical label attached to the product, whereas the storage requirements are typically located in the study protocol, which outlines the guidelines for the entire study. The CRF directions may provide information on how to record storage information, but not necessarily the specific requirements. The drug accountability log is a record of the product's usage, not storage requirements. Therefore, the most comprehensive source for storage requirements would be the study protocol.