Japanese Pharmacology & Therapeutics (JPT)
Vol. 47 Suppl. 1 2019
■ REVIEW Future Development of Pharmaceuticals and Medical Devices
Curent Status and Expectations of Diversification of Clinical Trials
H. Ohtsu
Jpn Pharmacol Ther 2019 47(s1) s6-8
A Background of "Proposal on Assuring the Reliability of Patient Registry Data for Use in Application Dossiers of Pharmaceuticals and Medical Devices"
T. Shibata
Research team for AMED Research on the Regulatory Science of Pharmaceuticals and Medical Devices:
Utilization of real world evidence using patient registry data to support regulatory decision-making.
Jpn Pharmacol Ther 2019 47(s1) s9-12
Proposal on Assuring the Reliability of Patient Registry Data for Use in Application Dossiers of Pharmaceuticals and Medical Devices.
[January 2019]
AMED Research on the Regulatory Science of Pharmaceuticals and Medical Devices
Title of research and development: Utilization of real world evidence using patient registry data to support regulatory decision-making
[Grant number JP18mk0101068]
Jpn Pharmacol Ther 2019 47(s1) s23-35
■ ORIGINAL ARTICLE
Patients' and Their Family's Information Needs and Reasons for Investigational Medical Care in Oncology:
Consultation Analysis from the Cancer Information and Support Centers
Y. Ogo, et al
Jpn Pharmacol Ther 2019 47(s1) s49-58
A Survey of Researchers on Clinical Trials Act
H. Kunitoh, et al
Jpn Pharmacol Ther 2019 47(s1) s59-66
■ BRIEF REPORT
Establishment of an Effective Monitoring Support System for ICH-GCP Compliant Trials
A. Saito, et al
Jpn Pharmacol Ther 2019 47(s1) s67-86
■ CASE REPORT
Current Status of Serious Adverse Event Report Contents in Investigator-initiated
Clinical Researches at Kanazawa University Hospital and Actions on Issues
N. Horikawa, et al
Jpn Pharmacol Ther 2019 47(s1) s87-93
■ REVIEW ARTICLE
How to Secure the Quality of the Clinical Trial Efficiently?
Cooperation among Clinical Data Managers
Y. Yamahara, et al
Jpn Pharmacol Ther 2019 47(s1) s94-101