Steps to conduct clinical trials

Author:

Peepliwal Ashok Kumar

Publisher

Elsevier

Reference44 articles.

1. Research regulations, ethics committees, and confronting global standards;Akabayashi,2020

2. A study to assess the completeness of informed consent documents for biomedical research on human participants submitted to the institutional ethics committee of a tertiary care hospital;Anandabaskar;International Journal of Basic & Clinical Pharmacology,2019

3. Logistics and supply chain management: An overview;Anca;Studies in Business and Economics,2019

4. Impact of source data verification on data quality in clinical trials: An empirical post hoc analysis of three phase 3 randomized clinical trials;Andersen;British Journal of Clinical Pharmacology,2015

5. A medication reconciliation form and its impact on the medical record in a paediatric hospital;Bédard;Journal of Evaluation in Clinical Practice,2011

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