Sterisart Universal Pump | How the 4th Generation - Advance Achieves Regulatory Compliance!
This document is a white paper summarizing the regulatory framework for the management of electronic records and electronic signatures in the pharmaceutical industry. It covers the full scope of the requirements outlined in 21 CFR Part 11. The aim is to provide a comprehensive understanding of these requirements, enabling the evaluation and enhancement of electronic record management practices in accordance with regulatory standards. [Contents (partial)] ■ Abstract ■ Regulations and their interpretation ■ Compliance with 21 CFR Part 11 ■ Controls in closed systems ■ Management of open systems *For more details, please download the PDF or feel free to contact us.
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【Other Published Content】 ■Explicit Signature ■Signature and Record Linking ■General Requirements ■Components and Management of Electronic Signatures ■Control of Identification Codes and Passwords *For more details, please download the PDF or feel free to contact us.
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Download All Catalogs![[Document] 21CFR Part 11 Compliance Checklist](https://image.mono.ipros.com/public/catalog/image/2049051/IPROS16528198867766470811.jpeg?w=120&h=170)
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Sartorius is a leading global company that contributes to biopharmaceutical research and the biopharmaceutical industry, established in 1870. Sartorius's laboratory products/services division meets the needs of researchers and technicians engaged in research and development and quality control in the medical industry and various other sectors by providing innovative laboratory equipment and consumables. Our products and technologies are designed to simplify our customers' operations and contribute to accelerating research and improving operational efficiency. *Biotechnology-related products can be found at the following URL: https://premium.ipros.jp/sartorius-stedim/
