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T/SHSPTA 001-2023 Active
T/SHSPTA 001-2023 The standard for supply chain management of clinical trial drugs
Abstract
This document stipulates the requirements for all relevant parties, personnel, facilities and equipment, digital information platforms, quality management, process management, and file management in the supply chain of drugs used in clinical trials. This document is applicable to the management of the supply chain of drugs used in clinical trials for drug registration applications. Other supply chains of drugs used in clinical research can also refer to and implement it.
General Product Information
| Document Type | Group standards |
|---|---|
| Standard Status | Active |
| Standard Code | T/SHSPTA 001-2023 |
| Implement Date | 1970-01-01 |
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