Essential information in protocols and pharmacy manuals for investigational drug services
This study highlighted a lack in clinical trial documentation of some elements required by IDS. Comprehensive documents may expedite pharmacy start-up of clinical trials. Thorough information is needed to support participant safety and data integrity. These documentation gaps underscore the need for improved collaboration between industry sponsors and IDS.
Authors
- Cynthia Tanguay (ORCID: https://orcid.org/0000-0003-0969-6051)
- Hélène Roy
- Catherine Côté-Sergerie
- Rachel Choquette
Institutions
- Centre Hospitalier Universitaire Sainte-Justine (CA)
Publication Details
- Journal
- American Journal of Health-System Pharmacy
- Published
- 2026-01-07
- DOI
- https://doi.org/10.1093/ajhp/zxag005
- Primary Topic
- Pharmaceutical studies and practices
- Type
- article
- Field-Weighted Citation Impact
- 0.00