A Practical Guide to Clinical Studies in Veterinary Oncology

Author:

Weishaar Kristen,Shiu Kai-Biu,Wright Zachary M.

Publisher

Elsevier BV

Subject

Small Animals

Reference9 articles.

1. International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH). Integrated addendum to ICH E6(R1): guideline for good clinical practice E6(R2). Step 4 version dated 9 November 2016. Available at: https://database.ich.org/sites/default/files/E6_R2_Addendum.pdf. Accessed August 8, 2023.

2. Investigator-initiated studies: Challenges and solutions;Konwar;Perspect Clin Res,2018

3. Data management in clinical research: An overview;Krishnankutty;Indian J Pharmacol,2012

4. An outline of data management in clinical research;Matkar;Int J Clin Trials,2017

5. FDA Guidance Document Part 11, Electronic Records; Electronic Signatures - Scope and Application. Available at: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/part-11-electronic-records-electronic-signatures-scope-and-application. Accessed August 8, 2023.

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