Digitalization of Battery Production

The Future of Battery Production

Delve into the transformative era of battery manufacturing, emphasizing sustainability, quality cont...

数据完整性网上技术交流讲座

数据完整性网上技术交流讲座

了解数据完整性标准和如何评估实验室数据管理过程,以确保符合法规要求。

Power the Bench - An Enhanced Strategy for Data Integrity

Power the Bench - An Enhanced Strategy for Data Integrity

Achieve workflow control, traceability and data automation by integrating bench top instruments and...

实验室数据管理指南

实验室数据
管理指南

《数据管理指南》为希望改进实验室数据管理的组织提供了策略。了解实施更好的管理规范的优点与挑战。

实验室数据可靠性指南

实验室数据可靠性指南

收集关于ALCOA+原理、SOP指南、数据管理和实用技巧的知识,以确保实验室中的数据可靠性。

21 CFR Part 11 Compliant Instruments

21 CFR Part 11 Compliant Instruments

Electronic Records on Instruments without a PC? Please read why experts state, that standalone instr...

Full compliance for 21 CFR part 11 and EU Annex 11

Full compliance for 21 CFR part 11 and EU Annex 11

Compliance for 21 CFR of FDA part 11 and EU Annex 11 regulations on electronic record submission is...

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