Adobe Sign合规性分析 21 CFR Part 11和Annex 11说明书 W H I T E P A P E R Adobe Sign An Analysis of Shared Responsibilities for 21 CFR Part 11 and Annex 11 Compliance
Validation package activities are intended to be executed using a configured Acrobat Sign enterprise plan service with SAML settings that are enabled for internal users to authenticate using their network credentials. The Acrobat Sign 21 CFR Part 11 validation package is available in English only and ...
If not, is it safe to say that only "digital signature" blocks used in (or added to) forms are considered Part 11 compliant? This would mean only 1 person could sign using the digital signature, correct (ie, it's locked down via checksum, etc, following signature 1 and another signat...
I'm also curious to know the difference between Adobe Sign and the free option in Adobe Reader to apply digital ID (certificates) in the light of 21 CFR part 11 compliance. Does the latter option allow for 21 cfr part 11 compliance? I'm really struggling with this. Most of...
Significantly accelerate the validation of Adobe's Acrobat Sign product against 21 CFR Part 11 & Annex 11 requirements with our documentation toolkit
2.法规遵从：该解决方案可以根据全球各地的行业特定法规进行配置，包括HIPAA、FERPA、GLBA和FDA 21 CFR part 11等，确保在不同行业和地区的合法合规使用。三、技术原理 1.公钥基础设施（PKI）Adobe Sign采用PKI体系来确保电子签名的安全性和可靠性。其关键部分如下：数字证书：由权威的CA机构颁发给用户，基于X.509 ...
Acrobat Sign for Microsoft 其他集成 合作伙伴管理的集成 Acrobat Sign 开发人员 REST API Webhook 支持和故障排除 客户支持资源 Adobe 致力于开发辅助工具,并力求在其产品和服务中提供此功能。为了消除信息技术壁垒,向残障人士提供各种新的机会,并鼓励开发有助于实现这些目标的技术,Adobe 一直在贯彻执行辅助功能法律、...
Acrobat Sign Solutions can also be configured to meet industry-specific regulations around the world, including HIPAA, FERPA, GLBA, and FDA 21 CFR part 11. The bottom line? With Adobe, they don’t need to worry.As a leader in digital experiences trusted by Fortune 500 companies around the...
運用Acrobat Sign,您將可建立支援 FDA 21 CFR Part 11 (為食品藥物管理局 (FDA) 電子紀錄與簽名規範) 規定的數位表單。 製作知情同意書就跟寫簡訊一樣簡單,只要放進文件中,即可送出取得病患的電子簽名。數位簽名既安全、便利又方便追蹤,您可確保試驗或治療計畫符合規定,病患也得到充分告知。此外在使用 Adobe 工...
運用Acrobat Sign,您將可建立支援 FDA 21 CFR Part 11 (為食品藥物管理局 (FDA) 電子紀錄與簽名規範) 規定的數位表單。 製作知情同意書就跟寫簡訊一樣簡單,只要放進文件中,即可送出取得病患的電子簽名。數位簽名既安全、便利又方便追蹤,您可確保試驗或治療計畫符合規定,病患也得到充分告知。此外在使用 Adobe 工...