Qualityze empowers life sciences companies to adopt electronic records and signatures securely, enhancing regulatory adherence with 21 CFR Part 11.
21 CFR Part 11 is a regulation of the United States Food and Drug Administration (FDA) that establishes requirements for electronic records and electronic signatures used in regulated industries.
21 CFR Part 11 compliant Quality Management Software offers businesses data integrity, security, and compliance in highly regulated industries like healthcare and pharmaceuticals. It ensures the reliability of electronic records and signatures, streamlining processes, reducing errors, and mitigating risks of non-compliance. Here are some of the advantages of having Qualityze, a 21 CFR Part 11 compliant QMS Software:
Qualityze ensures adherence to FDA requirements. It reduces the risk of non-compliance which lead to costly penalties and product recalls.
Qualityze enhances the integrity of electronic records and signatures, ensuring the accuracy and reliability of critical quality and compliance data.
Qualityze streamlines document management, version control, and approval processes, reducing errors and improving efficiency.
Qualityze facilitates secure and legally compliant electronic signatures, eliminating the need for physical paper signature and expediting the approval processes.
Qualityze provides robust audit trails, tracking all system activities and enabling transparency and accountability in the system.
Qualityze implements stringent access controls and data encryption measures to safeguard sensitive information and protect against data breaches.
Qualityze allows authorized personnel to access quality and compliance data from anywhere, facilitating remote work and global operations.
The specific elements of 21 CFR Part 11 that are supported by Qualityze may vary depending on the version and configuration of the software, as well as the specific modules or features used. However, based on the information provided earlier in this conversation, here's how Qualityze supports key elements of 21 CFR Part 11:
Sub-Part B: Electronic Records | ||
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11.10 11.30 | Controls for closed systems. Controls for open systems. |
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11.50 | Signature manifestations. | Electronic Signature Functionality. The system prompts the user to key-in the user id and password for create, edit, approve and delete actions within the system. When the create, edit, approval, reject and/or delete action is executed, the system captures:
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11.70 | Signature/record linking. | Audit Trail Functionality along with electronic signature functionality with Date & Time Stamping for all records related description. It ensures to capture details for each and every system entry done for all the records including the previous and current change value/description. |
Sub-Part B: Electronic Signatures | ||
11.100 | General requirements. | Electronic signature of a user is unique combination of a user-id and password. A user-id and associated with a user who can be further identified by their Name (FN, LN), Title, email address and a phone number (optional) in the system. |
11.200 | Electronic signature components and controls. | To gain access to the system, a user must input two distinct identification components:
Once logged in the system, any create, edit, approve, reject, delete action required re-entering the user-id and password combination. |
11.300: | Controls for identification codes/passwords. | User-id and password policy management is controlled by the designated administrator of the system.
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