Presentation on theme: "Overview of 21CFR Part 11: The Final Rule"— Presentation transcript:
1Overview of 21CFR Part 11: The Final Rule PERI ELECTRONIC RECORDSAND SIGNATURES WORKSHOPPhiladelphiaNovember 8, 1999Presentation by Daniel Worden
221 CFR Part 11 Electronic Records; Electronic Signature Milestones11/91 Project Launched7/92 Advanced Notice8/94 Proposed Rule3/97 Final Rule8/97 In EffectPaul Motise
3E - Record / E - Signature Acceptance ReliableTrustworthyPart 11Authentic & Legal
421 CFR Part 11 Electronic Records: Electronic Signature AGENDASummary of 21 CFR, Part 11Subpart A: General ProvisionsSubpart B: Electronic RecordsSubpart C: Electronic SignaturesPotential IssuesAdvantages and ChallengesCritical Success FactorsSecurity and Control
521 CFR Part 11 Electronic Records: Electronic Signature Subpart A - General ProvisionsSection 11.1 ScopeRegulations establish the criteria the FDA considers for electronic records and and electronic signature to be trustworthy, reliable, and generally equivalent to paper.Applies to all records in electronic form under any records requirement within any FDA regulation.Electronic records are considered equivalent to full handwritten signatures, initials, and other general signings.Electronic records may be used in accordance with Part 11 unless paper records are specifically required.Computer system (hardware and software), controls, and relevant documentation must be available for review during FDA inspections.
621 CFR Part 11 Electronic Records: Electronic Signature “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.”
721 CFR Part 11 Electronic Records: Electronic Signature “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.”
821 CFR Part 11 Electronic Records: Electronic Signature Handwritten Signature“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.”
921 CFR Part 11 Electronic Records: Electronic Signature Digital Signature“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.”Biometrics“A method of varifying 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.”
1021 CFR Part 11 Electronic Records: Electronic Signature Closed System“An environment in which system access is controlled by persons who are persons who are responsible for the content of electronic records that are on the system.”Open System“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.”
1121 CFR Part 11 Electronic Records: Electronic Signature Subpart B - Electronic RecordsSection Controls for Closed SystemsMust develop procedures and controls to ensure authenticity, integrity and confidentiality, and that signer cannot repudiate the signed record. The controls must:Be validatedMaintain accurate and complete recordsLimit the system to authorized personsProtect records through retention periodContain audit trails that are secure, operator independent, computer-generated, time-stamped, cover the creation , modification and deletion of records and do not obscure previous information
1221 CFR Part 11 Electronic Records: Electronic Signature Section Controls for Closed Systems (cont.)Allow for the performance of operational system checks, authority checks, and device checks to ensure system, record, and data integrityEnsure appropriate personnel qualificationsPolicies written and followed to hold personnel accountable for actions and to deter records falsificationControl over system documentation including distribution, access, use, revision and change control
1321 CFR Part 11 Electronic Records: Electronic Signature Section Controls for Open SystemsMust develop procedures and controls that ensure authenticity, integrity, and confidentiality of electronic records and comply with all other parts of Section 11.10Must use additional measures (e.g. document encryption, digital signature standards) to ensure authenticity, integrity, and confidentiality
1421 CFR Part 11 Electronic Records: Electronic Signature Section Signature ManifestationSigned electronic records must include the printed name of the signer, date and time of signature, and the purpose of the signature (e.g. review, approval etc.) Each of these must be readable by display or printout.Section Signature/Record LinkingElectronic signature and handwritten signatures must be linked to ensure signatures cannot be excised, copied, transferred or falsified.
1521 CFR Part 11 Electronic Records: Electronic Signature Subpart C-Electronic SignatureSection General RequirementsMust be unique to an individual and not reassignedIdentity of individual must be verified by organizationMust certify electronic signature system to the agency prior to or at the time of use of the systemCertification must be submitted in paper form and, upon agency request, provide certification that signature is legally binding
1621 CFR Part 11 Electronic Records: Electronic Signature Section Electronic Signature Components and ControlsNon-Biometric signatures must:Contain at least two different identification components (e.g. User ID and Password)Single sign-on with multiple tasks: Use all identification components at first, with partial identification for each task thereafterMultiple sign-on without continuous access requires all identification components to be used each timeBe used only by the ownerEnsure use by other individuals is precluded and does not occur without collaboration by at least two other individualsBiometric signatures must ensure use by the owner
1721 CFR Part 11 Electronic Records: Electronic Signature Section Controls for Identification Codes/PasswordsPersons using electronic signatures must use controls to ensure security and integrity and should include:Assuring that no two individuals have the same combination of identification code and passwordPeriodic check, recall, or revision of identification code and passwordLoss management and replacement proceduresTesting of devices (i.e. tokens or cards) that produce or maintain identification codes or passwords to ensure proper function and unaltered state.
1821 CFR Part 11 Electronic Records: Electronic Signature Section Controls for ID codes/passwordsUnauthorized use safeguardsReport attempts in urgent & immediate manner to:Security unitManagement, as appropriate
1921 CFR Part 11 Electronic Records: Electronic Signature FDA’s View of What Industry Needs to DoLearn Part 11File (c) CertificationE-records maintainedID formats FDA can audit/copyCheck with FDA auditorsWatch for guidance documents
20Part 11 Internet Web Site: 21 CFR Part 11 Electronic Records: Electronic SignaturePart 11 Internet Web Site:
2121 CFR Part 11 Electronic Records: Electronic Signature 7520 Standish PlaceRockville, MD 20855Paul J. MotiseConsumer Safety OfficerDivision of Manufacturing and Product Quality, HFD-320Center for Drug Evaluation and ResearchPhone: Fax:
22FORMULATE AN INFORMATION STRATEGY ENTERPRISE GOALSTime to Market“Quality” of DevelopmentLink to Market & Customer InformationOrganizational EffectivenessCross-functional process flowsCross-functional Information flowsContinuous Process ImprovementGlobal resource managementProcess ValidationRegulatory InterfaceAccelerated Review &ApprovalStandardized SubmissionsComputer ValidationSTRATEGIC PLANDRUG DEVELOPMENTINFORMATIONMANAGEMENTINFORMATION STRUCTURE ®ULATORY REQUIREMENTSDEVELOPMENT PROCESSGlobal Information ArchitectureApplication PortfolioEnabling Technologies/ToolsLegacy SystemsINFORMATION SYSTEMS TECHNOLOGY
23*GISP- Good Information APPLICABILITY OF PART 11-GXP Training-GXP Tracking-SOP SystemsGXP[ quality management systems ]GLPGCPGMPGISP *-Data Acquisition-Laboratory InformationManagement (LIMS)-Laboratory Robotics-Toxicology Systems-Stability Systems-Environmental Impact-Centralized Laboratory-Data Acquisition & Reporting-Remote Data Entry-Case Report Form Systems-Clinical Data management-Adverse Event Reporting-Clinical Supply Systems-Statistical Analysis Systems-Manufacturing Execution (MES)-Maintenance Management (MMS)-Calibration Management (MCS)-Facility Management Systems-Enterprise Resource Plan ( ERP)-SCADA Systems-Supply Chain Planning (SCP)-Internet Applications-EDI-PLC Systems-Document Management-Quality Management-Computer Assisted NDA(CANDA)*GISP- Good InformationSystem Practices
25THE FOUNDATION“The Agency believes that if it is important enough that a record be signed, human readable displays of such records must include the printed name of the signer, the date and time of signing, and the meaning of the signature”.Example: a message from a firm’s management to employees instructing them on a particular course of action may be critical in litigation.
26Potential IssuesThe final rule does not establish numerical standards for levels of security or validation (persons have the option of determining the frequency).Wide spread implementation of time date stamped audit trails executed objectively and automatically and controls for limiting access to the database search software may change a company’s current practices.The word “ensure” is used in the regulations. It is defined as “to make certain”. How will this be interpreted by a field inspector?“Unique nature of passwords”. How is uniqueness determined and what are “good password practices”?Part 11 does not apply to paper records that are or have been transmitted by electronic means but it does apply to records in electronic form that are created, modified, maintained, archived, retrieved under any record requirement regulated by FDA.Record retention requirements for software and hardware used to create records that are retained in electronic form are subject to part 11.
27Potential Issues (Cont’d) “As the agency’s experience with part 11 increases certain records may need to be limited to paper if there are problems with the electronic versions of such records.”“It may be necessary to inspect hardware and software used to generate and maintain electronic records to determine if the provisions of part 11 are being met.”The assessment of adequacy of systems validation will include inspection of hardware to “determine if it matches the system documentation description of the hardware.”For geographically dispersed systems, inspections would extend to operations, procedures and controls at one location and the agency would inspect other locations of the network in a separate but coordinated manner.Is the implementation of an electronic system significant enough in manufacturing to require an NDA supplement prior to going live?Dial-in access over public phone lines can be a closed system if access to the system is under the control of the persons responsible for the content of the record.
28Potential Issues (Cont’d) When an organization’s electronic records are stored on systems operated by third parties the agency would consider this to be an open system.Electronic record is defined as “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.”“The Agency believes that if it is important enough that a record be signed, human readable displays of such records must include the printed name of the signer, the date and time of signing, and the meaning of the signature”. Example: a message from a firm’s management to employees instructing them on a particular course of action may be critical in litigation.“A single certification may be stated in broad terms that encompass electronic signatures of all current and future employees”.
29Potential Issues (Cont’d) 21CFR11 applies only to those records required to be created, archived, and/or signed or initialed in accordance with another (predicate rule) FDA regulation. Failure to comply with Part 11 effectively invalidates the electronic record, thus placing the firm in violation of the predicate rule requiring the record.The FDA is being lenient in enforcing the rule unless the investigator has reason to question the integrity of the data.PhRMA feels that FDA’s interpretation of the electronic record portion of the rule is flawed since many computer systems in use in R&D, clinical and QC lack the capability of generating time-date audit trails (e.g.SAS and HPLC).21CFR11 has evolved from an approach to facilitate a paperless system into an FDA enforcement tool .PhRMA claims that the FDA definition of raw data has changed. Previous to the rule, raw data was considered to be paper documents with a handwritten signature. If the data were generated from a computer, the printout was signed and archived as the official record.
30Potential Issues (Cont’d) FDA is considering additional guidance to try to create a procedure to ensure that electronic records can not be changed after a hardcopy has been signed.FDA would like to obtain a copy of each electronic file, manipulate it, study it, and pick out trends.The transition to paperless systems has proven to be gradual and potentially very expensive. Industry, therefore, has opted to maintain hybrid systems because many systems currently in use in R&D and Manufacturing are not able to comply with the electronic signature section of Part 11.As of August 20, 1997 firms that used hybrid systems had the choice of maintaining the hybrids or converting to an electronic environment, in whole or in part, to meet FDA maintenance record requirements.ID’s should not be reused even if the person using the ID leaves the company.Passwords should consist of a minimum of six characters using a combination of letters and numbers.
31Certification Statement Pursuant to section of Title 21 of the code of Federal Regulations, thisis to certify that __________________ intends that all electronic signaturesName of organizationexecuted by our employees, agents, or representatives, located anywhere in theworld, are the legally binding equivalent of traditional handwritten signatures.
32Stringent Controls“The agency believes that…it is vital to have stringent controls in place to prevent impersonation. Such controls include: (1) requiring an individual to remain in close proximity to the workstation throughout the signing session; (2) use of automatic inactivity disconnect measures that would “de-log” the first individual if no entries or actions were taken within a fixed short timeframe; and (3) requiring that the single component needed for subsequent signings be known to, and usable only by, the authorized individual
33Electronic Signatures and Electronic Records AdvantagesElectronic Batch records can eliminate mountains of paper work, speed processing and allow for statistical and trend analyses.NDA’s and other submissions can be submitted electronically in place of paper submission.Increases the speed of information exchange.Cost savings from reduced need for storage space.Manufacturing process streamlining.Job creation in industries involved in electronic record and electronic signature technologies.ChallengesFirms planning on using electronic signatures in FDA regulated environments will be required to validate the computer related systems.Design of systems must be well thought out and tested thoroughly.Critical control points must be identified which can be monitored through electronic audit trails.Adequate testing of security.Fraud Detection
34Electronic Signatures and Electronic Documents Critical Success FactorsValidation activities in manufacturing, toxicology, clinical, regulatory and perhaps marketing (label approval) will need to be better process focussed, requiring definition of inputs and outputs with, procedural controls governing the process activities and standards dictating the format and content of inputs and outputs and well documented.Configuration management, security management and periodic review and quality management must be a continual process.Record retention and record disposal practices need to be revised to reflect company requirements to comply with new regulatory requirements.Documentation standards and practices should be created that systematize the processes for creating and maintaining documents.Planning will have to take into consideration re-engineering, replacement, or retirement of a computer system when operating costs increase or business process changes.Requires effective change control.
36Procedural - Verification Obtain and Review Corporate Security policy, security standards and proceduresEvaluate the effectiveness of the security organizationEvaluate the effectiveness of the process for requesting, granting and removing access.
37Physical Security Review Physical Access Policy Identify sensitive areas (computer room, data rooms, wiring closets).Determine process for granting, reviewing, monitoring and removing access.Verify that process is operating effectively.
38Logical Security Obtain and review data access policy Identify access “Paths” to cGMP dataDial-inInternetLocal Area NetworkOperating SystemDatabase SecurityApplication Security
39Logical Security For each access path, evaluate the following: user security parametersunique user ID/password combinationspassword change intervals (90 days)password composition (e.g., combination of numbers and letters required)password length (minimum length of 6 characters)access controls that enforce segregation of duties (read, write, delete)monitoring functionality and audit trail
40THE PATH FORWARD GAP ANALYSIS “As Is” processes Design Specs Risk ExposureSYSTEM CONTROLSSecurityElectronic Record RetentionMonitoringFRAUDMONITORING 483s
41QUESTIONS AND ANSWERS --FDA’s PAUL MOTISE  Questions and answers from Paul Motise at various industry meetings, as well as conversations and his updatesQ: Can a firm which maintains regulatory records in computer files be exempt from FDA’s signature rule if periodically the firm prints paper hard copies of all documents as it’s official record?A: Paul Motise says no. On 10/22/97 US District Judge Paul Friedman nullified a National Archives Regulation authorizing all Government Agencies to erase electronic documents if paper is archived. Example: Spreadsheet shows results but not the algorithm.Q: What must the audit trail contain?A: Date/time of operator entries that create, modify, or delete information and who did what, wrote what, and when.Q: Can an audit trail be paper?A: No. It must be a computer generated electronic record.Q: Must an audit trail be signed?A: No. It must be independent of the operator and operators must not be able to sign the audit trail.
42QUESTIONS AND ANSWERS --FDA’s PAUL MOTISE  Q: Will an electronic signature with only a date stamp be acceptable or does the time of day need to be included?A: Time is vital and must be included.Q: Do you really expect to have certifications from every regulated company as in part , even if they are only using electronic signatures for open systems (such as ) and are not using electronic signatures for collecting original data, authorizing documents or electronic submissions?A: Yes. We are asking for that certification from every company that is using an electronic signature to meet FDA signature requirements. It doesn’t matter if it is open or closed.Q: In the GLPs [Part 58.81(a)] the requirement is that changes to SOPs “be authorized in writing by management”. Does 21CFR11 broaden the meaning of “in writing” to include “be authorized in writing or electronically by management”?A. In GLPs, if you have a particular record, then Part 11 applies to the record. If you are going to create an endorsement electronically, then Part 11 applies. If a record is required by FDA then Part 11 applies.Q: If I scan in CRFs to get into a report and I will be signing the final report as the preparer of the submission, would that be acceptable to the agency?A. Yes. This is a hybrid system, but for the electronic record you will apply an electronic signature to the entire thing. What is signed should be protected so that later on nothing can be switched.
43MORE FROM THE FDAField Notice FMD /22/97 tells investigators to check the ORA Intranet site to determine if an electronic signature certification has been filed prior to arriving at the inspection site.Guidance to FDA Inspectors for Making and Maintaining Copies of Electronic Records:1) Use digital signature software to authenticate your copy file; signature verification would detect any post signing record changes.2) Obtain an affidavit from the firm confirming that the copy is accurate and complete.3) Place the disk or tape holding your electronic copy in a container under official seal and documenting a chain of custody for the container in a manner similar to official samples.