This document outlines a protocol for conducting a therapeutic drug monitoring study, including sections for the title, investigators, study location, patient recruitment details, need for the study, objectives, patient selection criteria, procedures for blood sample collection and storage, instruments for measuring drug and clinical levels, report preparation, clinical interpretation, and conclusion.

1. PROTOCOL
FOR
THERAPEUTIC DRUG MONITORING
SWARNA PRIYA B
JAYA COLLEGE OF PHARMACY,
THIRUNINRAVUR, CHENNAI

2. PROTOCOL
• TITLE OF THE STUDY/PROJECT
• INVESTIGATORS
Chief Investigator
Joint Investigator
Co Investigator – Clinical and Research Fellow
• PLACE OF THE STUDY
• PATIENT RECRUITMENT PLACE
• NEED FOR TDM STUDY
• OBJECTIVE OF THE STUDY

3. Cont.
• CRITERIA FOR SELECTION OF PATIENTS
• PATIENT HISTORY
• WITHDRAWAL OF BLOOD SAMPLE AND
STORAGE
• INSTRUMENT FOR
• Measurement of drug levels
• Measurement of clinical parameters (ECG, EEG,
RESPIRATION)
• REPORT PREPARATION
• CLINICAL INTERPRETATION

4. TITLE OF THE
STUDY/PROJECT

5. INVESTIGATORS
Chief Investigator
Joint Investigator
Co Investigator – Clinical and Research Fellow

6. PLACE OF THE STUDY

7. PATIENT RECRUITMENT
PLACE

8. NEED FOR TDM STUDY

9. OBJECTIVE OF TDM STUDY

10. CRITERIA OF THE STUDY

11. PATIENT HISTORY

12. WITHDRAWAL OF BLOOD
SAMPLE AND STORAGE

13. INSTRUMENT FOR
• Measurement of drug levels
• Measurement of clinical parameters (ECG, EEG, RESPIRATION)

14. REPORT PREPARATION

15. CLINICAL INTERPRETATION

16. CONCLUSION