Get Report On Receipt Of Drug - Guide For Reporting Investigational New - Fws

The Report On Receipt Of Drug - Guide For Reporting Investigational New - Fws is essential for accurately documenting the receipt of investigational new animal drugs. This guide will walk you through the process of filling out the form online, ensuring all required information is complete and accurate.

Follow the steps to fill out the Report On Receipt Of Drug form effectively.

1. Click the ‘Get Form’ button to obtain the form and launch it in your preferred document editor.
2. Begin by entering the name of the drug in the appropriate field. For example, enter ''.
3. Specify the proposed use of the drug, such as 'Treatment of certain bacterial diseases that occur in a variety of fish species'.
4. Enter the INAD Number in the designated section, which is '9332' for this example.
5. Fill in the date of the CVM authorization letter, which is 'August 12, 2002'.
6. Document the date of drug receipt accurately.
7. Record the amount of drug received.
8. Note the drug lot number.
9. Enter the study worksheet number, also '9332'.
10. Provide your name and address as the investigator.
11. Indicate the location of the trial.
12. Specify if this is a pivotal study by indicating 'yes' or 'no'.
13. Indicate if this is a non-pivotal study by indicating 'yes' or 'no'.
14. Enter the approximate number of treated animals.
15. Document the approximate number of control animals.
16. Record the number of animals used previously.
17. Enter the study protocol number, which is '9332'.
18. Indicate the approximate dates of the trial, including start and end dates.
19. Detail the species, size, and type of animals involved.
20. Specify the maximum daily dose and duration of the treatment.
21. Document the method(s) of administration, such as 'Medicated-feed'.
22. List the withdrawal period based on the guidelines provided.
23. Ensure both the investigator and the study monitor sign and date the form.
24. Complete any last fields as required, such as the date prepared and the names of reviewers.
25. Finally, save any changes, download, print, or share the completed form as necessary.

Ensure your compliance by filling out the necessary documents online now.