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![Japan's PMDA: Reporting ADR & Defects during Clinical Trials using e-Application Data System](https://static.wixstatic.com/media/nsplsh_2d6171385274416a546549~mv2.jpg/v1/fill/w_399,h_300,fp_0.50_0.50,q_90,enc_auto/nsplsh_2d6171385274416a546549~mv2.jpg)
Sharan Murugan
- Apr 2, 2023
- 1 min
Japan's PMDA: Reporting ADR & Defects during Clinical Trials using e-Application Data System
Recently Japan's the Ministry of Health, Welfare and Labour (MHLW) - Pharmaceuticals and Medical Devices Agency issued guidance “System...
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![Japan PMDA: Guidelines for Labeling of Codes on Containers to Identify Prescription Drugs & Med. Dev](https://static.wixstatic.com/media/6516fb_f73ee22e6ba242fd9d96f685737cc914~mv2.jpg/v1/fill/w_399,h_243,fp_0.50_0.50,q_90,enc_auto/6516fb_f73ee22e6ba242fd9d96f685737cc914~mv2.jpg)
Sharan Murugan
- Oct 9, 2022
- 1 min
Japan PMDA: Guidelines for Labeling of Codes on Containers to Identify Prescription Drugs & Med. Dev
Recently Japan's the Ministry of Health, Welfare and Labour (MHLW) - Pharmaceuticals and Medical Devices Agency issued a Notification...
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