Clinical Research Study Investigator’s Toolbox
The NIA Clinical Research Toolbox offers web-based resources, templates, forms, and guidelines to support investigators in clinical research, from study setup to data sharing.
Study drug/ treatment Any single drug or combination of drugs administered to the patient as part of the required study procedures; includes
Clinical Study Templates and Forms - National Institute of …
Jun 20, 2024 · This template aims to facilitate the development of Phase 2 and 3 clinical trial protocols that require a Food and Drug Administration (FDA) Investigational New Drug (IND) or Investigational Device Exemption (IDE) application.
Drug Study Format | PDF - Scribd
This document outlines a template for studying drugs, including spaces for the generic and brand name, classification, route of administration, dosage, frequency, and nursing responsibilities before, during, and after administration.
Clinical Trials e-Protocol Template/Tool - NIDCD
The clinical trials electronic protocol writing template/tool provides a useful format for NIH-funded Phase II and III clinical trials that are being conducted under an FDA Investigational New Drug (IND) or Investigational Device Exemption (IDE) Application.
This protocol template is a tool to facilitate the development of a research study protocol specifically designed for the investigator initiated studies. It contains sample text to assist
Drug Study Template | PDF - Scribd
The template includes spaces for the medication name, dosage, route of administration, frequency, indication, action, contraindications, adverse effects, and nursing implications.
Pharma - DRUG Study Template | PDF - Scribd
Pharma_DRUG Study Template - Free download as Word Doc (.doc / .docx), PDF File (.pdf), Text File (.txt) or read online for free. This document appears to be a drug study template for a nursing student to complete.
Drug-Study - DRUG STUDY TEMPLATE - Nursing - Drug Study Drug …
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Drug Study Format 2018 - template - Drug Study DRUG NAME …
(Highlight or emphasize adverse effects manifested by the patient by underlining the sign and symptoms) evaluate for the occurrence of any adverse effects associated with drug therapy. c. Restrict amount of drug available to patient.
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