T/SHQAP 013-2025 Active Group standards

T/SHQAP 013-2025 Technical requirements of digital traceability in the whole process of drug production — Manufacturing super control and data acquisition

T/SHQAP 013-2025 Technical requirements of digital traceability in the whole process of drug production — Manufacturing super control and data acquisition

Publish Date: 2025-08-08 Implement Date: 2025-09-08 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us
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Basic Information

Standard Code: T/SHQAP 013-2025
Standard Type: Group standards
Standard Status: Active
is_force_gb: no
CCS Name: Biological products and blood products
ICS Name: Other standards related to pharmaceutics
Publish Date: 2025-08-08
Implement Date: 2025-09-08

Scope

This document sets forth technical requirements for digital traceability in the collection and monitoring of production data for pharmaceutical manufacturers. It makes relevant provisions in the areas of data collection, data storage, real-time process monitoring, alarm management, and data management and operation and maintenance, with the aim of guiding pharmaceutical manufacturers in Shanghai to establish production data collection and monitoring systems that meet the requirements of the "Good Manufacturing Practice for Pharmaceutical Products (Revised in 2010)"

Development Information

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