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Standard Operating Procedures5.14.1 Investigational Product HandlingVersionV2.2Author/sB Fazes, S KochovskaApprovedD CurrowEffective date28/02/2018Review date31/12/2019DO NOT USE THIS SOP IN PRINTED
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Step 1: Review the newfinal5141 investigational product handling guidelines.
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Step 2: Identify the necessary materials and equipment for handling the investigational product.
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Step 3: Prepare a clean and sterile work area to ensure proper handling.
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Step 4: Follow the specific instructions for preparing, storing, and administering the investigational product.
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Step 5: Document all steps taken in handling the investigational product for regulatory purposes.

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Research staff responsible for managing investigational products
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Newfinal5141 investigational product handling refers to the procedures and guidelines for managing investigational products during a clinical trial.
The sponsor or the principal investigator of the clinical trial is required to file newfinal5141 investigational product handling.
Newfinal5141 investigational product handling can be filled out by providing complete and accurate information about the investigational product used in the clinical trial.
The purpose of newfinal5141 investigational product handling is to ensure the proper storage, distribution, and accountability of investigational products throughout the clinical trial.
Information such as the name of the investigational product, batch number, expiration date, storage conditions, and distribution records must be reported on newfinal5141 investigational product handling.
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