Regulatory Considerations for Combined Drug-Device Studies in Europe: A Case Study Involving Bile Sampling
- DOI
- 10.1007/s40290-026-00619-9
- Published
- 2026-07-03
- Container
- Pharmaceutical Medicine
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1007/s40290-026-00619-9,
title = {Regulatory Considerations for Combined Drug-Device Studies in Europe: A Case Study Involving Bile Sampling},
author = {Hans-Peter Podhaisky and Emiko Tsuruta and Isabel Piel and Christiane Otto and Sofia Busto Paez and Miriam Font-Nieves},
year = {2026},
journal = {Pharmaceutical Medicine},
doi = {10.1007/s40290-026-00619-9},
url = {https://doi.org/10.1007/s40290-026-00619-9}
}RIS
TY - JOUR TI - Regulatory Considerations for Combined Drug-Device Studies in Europe: A Case Study Involving Bile Sampling AU - Hans-Peter Podhaisky AU - Emiko Tsuruta AU - Isabel Piel AU - Christiane Otto AU - Sofia Busto Paez AU - Miriam Font-Nieves PY - 2026 JO - Pharmaceutical Medicine DO - 10.1007/s40290-026-00619-9 UR - https://doi.org/10.1007/s40290-026-00619-9 ER -
APA
Podhaisky, H., Tsuruta, E., Piel, I., Otto, C., Paez, S. B., & Font-Nieves, M. (2026). Regulatory Considerations for Combined Drug-Device Studies in Europe: A Case Study Involving Bile Sampling. Pharmaceutical Medicine. https://doi.org/10.1007/s40290-026-00619-9
Source records
- crossref · retrieved 2026-11-04T02:28:48.964Z