CFR21第11部分

CFR21第11部分




English (Original Text)

A General Provisions

§ 11.1 Scope.

(a) The regulations in this part set

forth the criteria under which the

agency considers electronic records,

electronic signatures, and handwritten

signatures executed to electronic

records to be trustworthy, reliable, and

generally equivalent to paper records

and handwritten signatures executed on paper.

(b) This part applies to records in

electronic form that are created,

modified, maintained, archived,

retrieved, or transmitted, under any

records requirements set forth in agency

regulations. This part also applies to electronic

records submitted to the agency under

requirements of the Federal Food, Drug, and

Cosmetic Act and the Public Health Service Act,

even if such records are not specifically

identified in agency regulations.

However, this part does not apply to

paper records that are, or have been,

transmitted by electronic means.

(c) Where electronic signatures and

their associated electronic records meet the

requirements of this part, the agency will consider

the electronic signatures to be equivalent to full

handwritten signatures, initials, and other general

signings as required by agency regulations, unless

specifically excepted by regulation(s) effective on

or after august 20, 1997.

(d) Electronic records that meet the

requirements of this part may be used in lieu of

paper records, in accordance

with § 11.2, unless paper records are

specifically required.

(e) Computer systems (including

hardware and software), controls, and

attendant documentation maintained

under this part shall be readily available

for, and subject to, FDA inspection.

§ 11.2 Implementation

(a) For records required to be

maintained but not submitted to the

agency, persons may use electronic

records in lieu of paper records or

electronic signatures in lieu of

traditional signatures, in whole or in

part, provided that the requirements of

this part are met.

(b) For records submitted to the

agency, persons may use electronic

records in lieu of paper records or

electronic signatures in lieu of

traditional signatures, in whole or in

part, provided that:

(1) The requirements of this part are

met; and

(2) The document or parts of a

document to be submitted have been

identified in public docket No. 92S–

0251 as being the type of submission the agency

accepts in electronic form. This docket will identify

specifically what types of documents or parts of

documents are acceptable for

submission in electronic form without

paper records and the agency receiving

unit(s) (e.g., specific center, office,

division, branch) to which such

submissions may be made. Documents

to agency receiving unit(s) not specified

in the public docket will not be

considered as official if they are

submitted in electronic form; paper

forms of such documents will be

considered as official and must

accompany any electronic records.

Persons are expected to consult with the intended

agency receiving unit for

details on how (e.g., method of

transmission, media, file formats, and

technical protocols) and whether to

proceed with the electronic submission.

§ 11.3 Definitions.

(a) The definitions and interpretations

of terms contained in section 201 of the

act apply to those terms when used in

this part.

(b) The following definitions of terms

also apply to this part:

(1) Act means the Federal Food, Drug,

and Cosmetic Act (secs. 201–903 (21

U.S.C. 321–393)).

(2) Agency means the Food and Drug

Administration.

(3) Biometrics means a method of

verifying an individual’s identity based

on measurement of the individual’s

physical feature(s) or repeatable

action(s) where those features and/or

actions are both unique to that

individual and measurable.

(4) Closed system means an

environment in which system access is

controlled by persons who are

responsible for the content of electronic

records that are on the system.

(5) Digital signature means an

electronic signature based upon

cryptographic methods of originator

authentication, computed by using a set

of rules and a set of parameters such

that the identity of the signer and the

integrity of the data can be verified.

(6) Electronic record means any

combination of text, graphics, data,

audio, pictorial, or other information

representation in digital form that is

created, modified, maintained, archived, retrieved,

or distributed by a computer system.

(7) Electronic signature means a

computer data compilation of any

symbol or series of symbols executed,

adopted, or authorized by an individual

to be the legally binding equivalent of

the individual’s handwritten signature.

(8) Handwritten signature means the

scripted name or legal mark of an

individual handwritten by that

individual and executed or adopted

with the present intention to

authenticate a writing in a permanent

form. The act of signing with a writing

or marking instrument such as a pen or

stylus is preserved. The scripted name

or legal mark, while conventionally

applied to paper, may also be applied to other

devices that capture the name or mark.

(9) Open system means an environment in which

system access is

not controlled by persons who are

responsible for the content of electronic

records that are on the system.

Subpart B Electronic Records

B §11.10 Controls for closed systems.

Persons who use closed systems to create,

modify, maintain, or transmit electronic records

shall employ procedures and controls designed to

ensure the authenticity, integrity, and, when

appropriate, the confidentiality of electronic

records, and to ensure that the signer cannot

readily repudiate the signed record as not

genuine. Such procedures and controls shall

include the following:

11.10 (a) Validation of systems to ensure

accuracy, reliability, consistent intended

performance, and the ability to discern invalid or

altered records.

11.10 (b) The ability to generate accurate and

complete copies of records in both human

readable and electronic form suitable for

inspection, review, and copying by the agency.

Persons should contact the agency if there are

any questions regarding the ability of the agency

to perform such review and copying of the

electronic records.

11.10 (c) Protection of records to enable their

accurate and ready retrieval throughout the

records retention period

11.10 (d) Limiting system access to authorized

individuals.

11.10 (e) Use of secure, computer-generated,

time-stamped audit trails to independently record

the date and time of operator entries and

actions that create, modify, or delete electronic

records. Record changes shall not obscure

previously recorded information.

Such audit trail documentation shall be retained

for a period at least as long as that required for the

subject electronic records

and shall be available for agency review and

copying.

11.10 (f) Use of operational system checks to

enforce permitted sequencing of steps and events,

as appropriate.

11.10 (g) Use of authority checks to ensure that

only authorized individuals can use the system,

electronically sign a record, access the operation

or computer system input or output device, alter a

record, or perform the operation at hand.

11.10 (h) Use of device (e.g., terminal) checks to

determine, as appropriate, the validity of the

source of data input or operational instruction.

11.10 (i) Determination that persons who develop,

maintain, or use electronic record/electronic

signature systems have the education,

training, and experience to perform their assigned

tasks.

11.10 (j) The establishment of, and adherence to,

written policies that hold individuals accountable

and responsible for actions initiated under their

electronic signatures, in order to deter record and

signature falsification.

11.10 (k) Use of appropriate controls over systems

documentation including:

(1) Adequate controls over the distribution of,

access to, and use of documentation for system

operation and maintenance.

(2) Revision and change control procedures to

maintain an audit trail that documents time-

sequenced development and modification of

systems documentation.

B §11.30 Controls for open systems.

Persons who use open systems to create, modify,

maintain, or transmit electronic records shall

employ procedures and controls designed to

ensure the authenticity, integrity, and, as

appropriate, the confidentiality of electronic

records from the point of their creation to the point

of their receipt. Such procedures and controls

shall include those identified in §11.10, as

appropriate, and additional measures such as

document encryption and use of appropriate

digital signature standards to ensure, as

necessary under the circumstances, record

authenticity, integrity, and confidentiality.

B §11.50 Signature manifestations.

11.50 (a) Signed electronic records shall contain

information associated with the signing that clearly

indicates all of the following:

(1) The printed name of the signer;

(2) The date and time when the signature was

executed; and

(3) The meaning (such as review, approval,

responsibility, or authorship) associated with the

signature.

11.50 (b) The items identified in paragraphs (a)(1),

(a)(2), and (a)(3) of this section shall be subject to

the same controls as for electronic records and

shall be included as part of any human readable

form of the electronic record (such as electronic

display or printout).

B §11.70 Signature/record linking.

Electronic signatures and handwritten signatures

executed to electronic records shall be linked to

their respective electronic records to ensure that

the signatures cannot be excised, copied, or

otherwise transferred to falsify an electronic record

by ordinary means.

Subpart C Electronic signatures

C §11.100 General requirements.

11.100 (a) Each electronic signature shall be

unique to one individual and shall not be reused

by, or reassigned to, anyone else.

11.100 (b) Before an organization establishes,

assigns, certifies, or otherwise sanctions an

individual's electronic signature, or any element of

such electronic signature, the organization shall

verify the identity of the individual.

11.100 (c) Persons using electronic signatures

shall, prior to or at the time of such use, certify to

the agency that the electronic signatures in their

system, used on or after August 20, 1997, are

intended to be the legally binding equivalent of

traditional handwritten signatures.

(1) The certification shall be submitted in paper

form and signed with a traditional handwritten

signature, to the Office of Regional Operations

(HFC-100), 5600 Fishers Lane, Rockville, MD

20857,0

(2) Persons using electronic signatures shall, upon

agency request provide additional certification or

testimony that a specific electronic signature is the

legally binding equivalent of the signer's

handwritten signature.

C §11.200 Electronic signature components

and controls.

11.200 (a) Electronic signatures that are not

based upon biometrics shall

(1) Employ at least two distinct identification

components such as an identification code and

password.

11.200 (a)(1)(i) When an individual executes a

series of signings during a single, continuous

period of controlled system access, the firs

signing shall be executed using all electronic

signature components; subsequent signings shall

be executed using at least one electronic

signature component that is only executable by,

and designed to be used only by, the individual.

11.200 (a)(1)(ii) When an individual executes one

or more signings not performed during a single,

continuous period of controlled system access,

each signing shall be executed using all of the

electronic signature components.

11.200 (a)(2) Electronic signatures that are not

based upon biometrics shall be used only by their

genuine owners.

11.200 (a)(3) Be administered and executed to

ensure that attempted use of an individual's

electronic signature by anyone other than its

genuine owner requires collaboration of two or

more individuals.

11.200 (b) Electronic signatures based upon

biometrics shall be designed to ensure that they

cannot be used by anyone other than their

genuine owners.

C §11.300 Controls for identification

codes/passwords.

Persons who use electronic signatures based

upon use of identification codes in combination

with passwords shall employ controls to ensure

their security and integrity. Such controls shall

include:

11.300 (a) Maintaining the uniqueness of each

combined identification code and password, such

that no two individuals have the same combination

of identification code and password.

11.300 (b) Ensuring that identification code and

password issuances are periodically checked,

recalled, or revised (e.g., to cover such events as

password aging).

11.300 (c) Following loss management

procedures to electronically deauthorize lost,

stolen, missing, or otherwise potentially

compromised tokens, cards, and other devices

that bear or generate identification code or

password information, and to issue temporary or

permanent replacements using suitable, rigorous

controls.

11.300 (d) Use of transaction safeguards to

prevent unauthorized use of passwords and/or

identification codes, and to detect and report in an

immediate and urgent manner any attempts at

their unauthorized use to the system security unit,

and, as appropriate, to organizational

management.

11.300 (e) Initial and periodic testing of devices,

such as tokens or cards, that bear or generate

identification code or password information to

ensure that they function properly and have not

been altered in an unauthorized manner.






德语翻译/德语翻译

A 部分 一般要求
§ 11.1 范围
(a) 本部分的指南规定了

当局在何种条件下

电子记录,电子记录
签名和手写签名
进行电子记录,如
值得信赖、可靠且总体而言
与纸质文档同义
考虑在纸上签署的签名。

(b) 本部分适用于电子
创建、修改、维护的记录,
存档、恢复或传输
成为并在任何
监管记录保存要求
指导方针下降。本部分也适用于
电子记录保存在
根据要求的权限
联邦食品和药品法
和化妆品等等
提交《国家卫生服务法》
即使没有这样的记录
权威指南中特别提到。
尽管如此,本部分不适用于
纸质记录转换为电子记录
被传送或被传送。

(c) 无论何时电子签名和
他们的相关电子记录
满足本部分的要求,
授权电子签名为
被视为等同于完全广告
手写签名、缩写和
其他通过的一般签名
需要监管要求
除非明确表示
于以下时间或之后出现异常
本指引自1997年8月20日起有效。

(d) 包含以下内容的电子记录
满足本部分要求的可发送至
纸质记录的地点
按照第 11.2 条使用,
除非纸质记录
是明确要求的。

(e) 计算机系统(包括硬件和
软件)、控制装置和随附的
属于此规则的文档,
应免费提供并接受 FDA 检查。

§11.2 实施

(a) 对于保存的记录
必须,但未提交给当局
个人可以
电子记录代替
纸质文件或电子文件
签名代替传统签名
全部或部分签名
使用,前提是
满足本部分的要求。

(b) 对于政府提交的记录,
个人可以电子化
记录代替纸质文件
和电子签名代替
完整或部分传统签名
使用共享的条件是:
(1)满足本部分的要求;和
(2) 文件或文件的一部分
公开提交的文件
官方可接受的案卷编号 92S-0251
接受电子提交表格。
该摘要清楚地阐明了什么样的
文件或部分文件
提交于
电子表格,无纸质文件
是可以接受的并且是官方机构。
提交的(例如特殊中心,
办公室、部门或分支机构)。文件
不属于官方机构
未指定公共摘要
被视为官方文件,如果它们在
以电子方式提交;
此类文档的纸质格式称为
正式考虑并且必须全部电子化
附带记录。预计
人们处理预期的事情
接收官方机构关于
有关细节的建议(例如转账方式、
媒体、文件格式和技术协议)
以及是否电子归档
是要进行的。
§11.3 定义

(a) 该法第 201 条规定的内容
此处包含的术语的定义和解释适用于这些术语包含在
可以用在这部分。

(b) 下列定义也适用于本部分:
(1) 法律是指联邦法律
食品、药品和化妆品(法案 201-
903(21 USC 321-393))。
(2) 权威是指食品和
药物管理局
(3) 生物识别技术是指一种方法
基于个人身份的验证
关于个人体能测量
特征或可重复的动作
这些特征和/或动作都
因人而异且可衡量
是。
(4) 封闭系统是指一个
可以访问系统的环境
对内容负责的人员受到控制
位于系统上的记录
有责任。
(5)数字签名是指一
电子签名基于
版权的加密方法
认证由一组计算得出
规则和一组参数
签字人的身份
并验证数据的完整性
能。
(6) 电子记录是指任何
文本、图形、数据、音频的组合,
数字形式的图像或其他信息,
它创建、更改、维护、存档,
恢复或通过计算机系统
是分布式的。
(七)电子签名是指
任何的计算机可读翻译
符号或一系列符号
执行、接受或由
个人已获得授权且合法
个人的有效等价物
手写签名。
(8) 手写签名是指
手写姓名或合法姓名
此人的有效缩写
当前打算以永久形式验证文件,
被执行或接受。这
执行签名
书写工具,例如笔筒或
保留了一支圆珠笔。这
书面姓名或合法有效的姓名
缩写也可以写在纸上
传输到其他输入/输出设备
将是这个名字或角色
可以保存。
(9) 开放系统是指一个环境
哪个系统访问不是通过
人们对此进行了检查
系统现有电子
记录负责。

B 部分电子记录

B §11.10 封闭系统的控制。
使用封闭系统的人
创建电子记录
改变、维持或转移
应用如此的程序和控制
设计、真实性、完整性以及在哪里
电子信息的保密性是必要的
以确保记录和
确保签字人拥有
签署记录并非如此
可以真实识别。这样的程序
和控制措施应包括以下内容:

11.10 (a) 系统验证
确保准确性、可靠性、
一致的预期性能,以及
能力无效或改变
识别记录。

11.10 (b) 正确和完整的能力
人类记录的副本
制作可读的电子表格,
供检查、审查和复制
经主管机关认定适合。人们应该
联系当局(如有)
有关当局能力的问题
此类支票和副本通过
进行电子记录

11.10(c) 保护记录以便正确使用
和期间的操作访问
文件保存期限
确保

11.10(d) 限制系统访问
获授权人士

11.10(e) 使用安全计算机
生成的、带有时间戳的审计跟踪
无论日期和时间
记录并接收操作员输入
需要电子记录的行动
创建、更改或删除。变化
记录的数量不应该是结果
隐藏以前记录的信息。
此类审计跟踪文件至少应
保留至此为止
适当的电子记录和
应提交给主管部门进行检查,并且
可以复印。

11.10 (f) 使用程序测试
系统以允许的顺序
强制执行的步骤和事件
必要的。

11.10(g) 使用访问测试
确保只有授权用户才能使用系统,文件
电子签名,访问
操作或计算机系统输入/输出设备
有、更改录音或
来开展当前的活动。

11.10 (h) 输入/输出设备的使用
如有必要,进行测试(例如终端键盘)
数据输入源或其中之一的有效性
来确定命令。

11.10 (i) 确定以下人员:
电子录音
/ 开发、维护或签名系统
利用正确的教育、培训和
有相关领域的经验
执行任务。

11.10 (j) 以书面形式设立和遵守
个人负责的既定规范
由他们的签名触发的操作
被追究责任和责任
伪造记录和
防止签名。

11.10 (k) 实施适当的控制
系统文档,包括:
(1) 对分销进行充分的控制,
访问和使用文档
系统运行和维护。
(2) 版本和变更控制程序,以维护显示时间的审计跟踪
的发展与变化
系统文档描述。

B §11.30 开放系统的控制。

使用开放系统的人们
创建电子记录
改变、维持或转移
应用程序和控制
真实性、完整性以及必要时
电子记录的保密性
从它的创造地到发生地
确保接待。
此类程序和控制措施应包括第 11.10 条中规定的程序和控制措施,以及必要时的其他措施,例如
文档加密及使用
合适的数字签名标准
包括适应情况
真实性、完整性和保密性
确保记录。

B §11.50 签名出场

11.50(a) 签署的电子版
记录应与
签署以下所有信息
包含:
(1) 申请人全名
签字人;
(2) 收到签名的日期和时间
已执行;和
(3) 与签名相关的
含义(例如审查、批准、
责任或作者身份)。
11.50 (b) (a)(1)、(a)(2) 款的规定
和 (a)(3) 描述的条款
部分应具有相同的控件
受到类似电子的影响
记录并应该成为每个人的一部分
人类可读的电子形式
可以包括录音(例如
电子显示或打印输出)

B §11.70 连接签名/文档

电子签名和
在一张上手写签名
进行电子记录,
应链接到相应的录音
将确保
签名未剪下、复印
或以其他方式转移到一个
通过正常方式进行电子记录
假的。

C 部分电子签名

C §11.100 一般要求

§11.100(a) 任何电子签名均应
对于一个人来说是并且应该是独一无二的
未被他人重复使用
或分配给另一个人。

§11.100(b) 在组织面前
电子签名或任何
电子签名的要素
人建立、分配、证明或记录
另有批准的,该人的身份
被检查的人。

§11.100 (c) 使用电子设备的人
使用的签名应在使用之前或使用时向当局证明:
您系统中的电子签名,
1997 年 8 月 20 日或之后使用
被认为具有与传统手写签名同等的法律约束力。
(1) 证明应为手写体
以纸质形式签署并发送
到:
区域运营办公室 (HFC-100), 5600
费舍尔巷,罗克维尔,MD 20857。
(2)电子签名的使用者
应根据官方要求使用
附加证书或证书
交付特定的电子
签署具有法律约束力的文件
相当于手写签名
签署人的。

C §11.200 电子元件
签名和控制

11,200

(a) 电子签名不
应基于生物识别程序:
(1) 至少两个不同的组件
用于身份识别,例如
识别码和密码

11,200 (a)(1)(一)
如果一个人有一个
单一期间的一系列签名,
受控的连续会话
系统访问应该是第一个签名
包含所有电子签名组件
被处决;以下签名
可以使用进行
至少一个组件只能通过
可以由该用户执行等等
设计为只能由该个人使用
可以使用。

11,200 (a)(1)(ii)
如果一个人有一个
或执行多个签名
在单个连续会话期间
提供受控的系统访问,
每个签名应包含所有相关文件
提供签名组件。

11,200(一)(2)
电子签名
不基于生物识别方法,只能由真实所有者使用。

11,200(一)(3)
以这样的方式应用和执行
确保尝试使用
真实签名之外的其他人对某人的电子签名
业主两人或两人合作
需要更多的人。

11,200(二)
基于电子签名
生物识别方法的设计应确保它们不会被真实方法以外的任何人使用
楼主可以用。

C§11.300
识别码控制
和密码。
使用电子签名的人
应使用基于识别码和密码的控制措施
应用以确保其安全性和完整性
确保。此类控制措施应
包括:
11,300(一)
保持个体的独特性
识别码和的组合
密码所以不能是两个人
相同的识别码组合
并有一个密码。

11,300(二)
确保获奖
识别码和密码
定期检查、召回或修订(例如,涵盖密码老化的情况)
11,300
遵守损失管理
对丢失、被盗、丢失或以其他方式受损的“令牌”(芯片卡)进行电子取消授权的程序,
卡和其他输入/输出设备,
识别码或密码信息
使用严格的控制来携带或生成并创建临时或永久的替代品。
11,300(天)
使用交易
采取措施防止和检测未经授权使用密码和/或识别码,并立即紧急解决任何未经授权的使用尝试
用于系统备份单元和
必要时向上级单位报告。
11,300(电子)
初步和定期审查
输入/输出设备,例如“令牌”(芯片卡)或卡,其中包含识别码或
携带或生成密码信息
可以,确保功能正确并且没有未经授权的更改
被制造了。

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