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Bulk Actions Log
The bulk actions log provides an easy way for administrators to track different bulk actions, such as uploading multiple users, envelope transfers, and publish envelope actions, for their account along with the progress and details of the actions.
To view the Bulk Actions Log, in DocuSign Admin, click Bulk Actions.
The view shows a list of bulk actions for your account. The type of action summary of the action, status, the name of the administrator that initiated the action, and the date of the action are listed.
When an action is complete, you can click Details, in the Summary, to review the information associated with the action and download a copy of the comma separated value (CSV) file with the information for the action. The Details information can include any error messages associated with the action.
You can also download the CSV file without reviewing any of the details.
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New DocuSign Experience Administrator Guide 179
DocuSign Part 11 Module Overview
DocuSign has partnered with industry experts to deliver transactions which meet the United
States Federal Food and Drug Administration (FDA) regulations. DocuSign's Part 11 module contains industry-designed capabilities that include: l
Pre-packaged account configuration l
Signature-level credentialing l
Signature-level Signing Reason l
Signature manifestation (Printed Name, Time Stamp, and Signature Reason) l
Detailed audit trail l
Tamper-evident digital seal using open PKI standards
DocuSign's Part 11 module enables customers to maintain compliance with national and international standards. DocuSign provides a high availability, high-security, and highly customizable solution which provides both electronic and digital signature (PKI) capabilities.
The module is configured in a standards compliant manner, allowing customers to benefit from efficiencies and cost-savings afforded by maintaining a digital process provides while ensuring compliance with standards in a systematic and controlled manner.
This section provides information about the account settings used by the DocuSign Part 11 module, which is designed to assist in compliance with FDA Title 21 of the Code of Federal
Regulations (CFR), Part 11. This guide also provides information about customer responsibilities for compliance; however these are only suggestions for the DocuSign portion of the 21 CFR Part
11 technology solution. Full compliance with 21 CFR Part 11 cannot be achieved with technology alone; it can be achieved through technology coupled with policies and procedures to ensure compliance. THIS INFORMATION IS NOT OFFERED AS LEGAL ADVICE.
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