Meeting Regulatory Requirements In Japan: Customised IXRS® Manages Patient-Specific Drug Orders
Japan’s clinical trial environment poses unique requirements and challenges. This informative case study uncovers how a top global pharmaceutical company was able to easily navigate and comply with the stringent management, shipping, and record keeping requests enforced by local Japanese regulatory standards.
You will discover:
- Interactive Response Technology (IRT) strategies for time-sensitive shipments
- Accommodations for managing bulk drug supply
- Ways of reducing response times to issues that arise daily
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