Thermo Scientific Qtegra Intelligent Scientific Data Solution (ISDS) Software for 21 CFR Part 11 Compliant Laboratories



Similar documents
How To Control A Record System

Implementation of 21CFR11 Features in Micromeritics Software Software ID

21 CFR PART 11 ELECTRONIC RECORDS, ELECTRONIC SIGNATURES CFR Part 11 Compliance PLA 2.1

FILEHOLD DOCUMENT MANAGEMENT SYSTEM 21 CFR PART 11 COMPLIANCE WHITE PAPER

POLICY ISSUES IN E-COMMERCE APPLICATIONS: ELECTRONIC RECORD AND SIGNATURE COMPLIANCE FDA 21 CFR 11 ALPHATRUST PRONTO ENTERPRISE PLATFORM

Self-Assessment of eresearch Compliance with 21 CFR Part 11, Electronic Record; Electronic Signatures

Compliance Matrix for 21 CFR Part 11: Electronic Records

Oracle WebCenter Content

Electronic records and electronic signatures in the regulated environment of the pharmaceutical and medical device industries

The Impact of 21 CFR Part 11 on Product Development

FDA Title 21 CFR Part 11:Electronic Records; Electronic Signatures; Final Rule (1997)

InfoCenter Suite and the FDA s 21 CFR part 11 Electronic Records; Electronic Signatures

A ChemoMetec A/S White Paper September 2013

Full Compliance Contents

Tools to Aid in 21 CFR Part 11 Compliance with EZChrom Elite Chromatography Data System. White Paper. By Frank Tontala

SolidWorks Enterprise PDM and FDA 21CFR Part 11

21 CFR Part 11 Implementation Spectrum ES

InfinityQS SPC Quality System & FDA s 21 CFR Part 11 Requirements

Intland s Medical Template

Enabling SharePoint for 21 CFR Part 11 Compliance - Electronic Signature Use Case

21 CFR Part 11 White Paper

Implementing CitectSCADA to meet the requirements of FDA 21 CFR Part 11

Agilent MicroLab Software with Spectroscopy Configuration Manager and Spectroscopy Database Administrator (SCM/SDA)

21 CFR Part 11 Electronic Records & Signatures

Implement best practices by using FileMaker Pro 7 as the backbone of your 21 CFR 11 compliant system.

FDA 21 CFR Part 11 Electronic records and signatures solutions for the Life Sciences Industry

Software Manual Part IV: FDA 21 CFR part 11. Version 2.20

DeltaV Capabilities for Electronic Records Management

AutoSave. Achieving Part 11 Compliance. A White Paper

For technical assistance, please contact: Thermo Nicolet Corporation 5225 Verona Road Madison WI

rsdm and 21 CFR Part 11

21 CFR Part 11 Checklist

Implementing Title 21 CFR Part 11 (Electronic Records ; Electronic Signatures) in Manufacturing Presented by: Steve Malyszko, P.E.

Empower TM 2 Software

DeltaV Capabilities for Electronic Records Management

Compliance Response Edition 07/2009. SIMATIC WinCC V7.0 Compliance Response Electronic Records / Electronic Signatures. simatic wincc DOKUMENTATION

21 CFR Part 11 Compliance Using STATISTICA

Meeting the FDA s Requirements for Electronic Records and Electronic Signatures (21 CFR Part 11)

Thermo Scientific ClinQuan MD Software For In Vitro Diagnostic Use. Confidence in Results With Data Integrity

Assessment of Vaisala Veriteq vlog Validation System Compliance to 21 CFR Part 11 Requirements

21 CFR Part 11 Deployment Guide for Wonderware System Platform 3.1, InTouch 10.1 and Historian 9.0

ScreenMaster RVG200 Paperless recorder FDA-approved record keeping. Measurement made easy

Nova Southeastern University Standard Operating Procedure for GCP. Title: Electronic Source Documents for Clinical Research Study Version # 1

Life sciences solutions compliant with FDA 21 CFR Part 11

Compliance in the BioPharma Industry. White Paper v1.0

Declaration of Conformity 21 CFR Part 11 SIMATIC WinCC flexible 2007

Compliance Response SIMATIC SIMATIC PCS 7 V8.1. Electronic Records / Electronic Signatures (ERES) Edition 03/2015. Answers for industry.

Software. For the 21 CFR Part 11 Environment. The Science and Technology of Small Particles

Using the Thermo Scientific Dionex Chromeleon 7 Chromatography Data System (CDS) to Comply with 21 CFR Part 11. Compliance Guide

Waters Empower 2 Software Seamlessly Manages Regulated Data to Aid in 21 CFR Part 11 Compliance

Waters Empower Software Seamlessly Manages Regulated Data to Aid in 21 CFR Part 11 Compliance

Electronic Document and Record Compliance for the Life Sciences

Data Management PACT Workshop: Design & Operation of GMP Cell Therapy Facilities April 10 th -11 th, 2007

Thermo Scientific Compound Discoverer Software. A New Generation. of integrated solutions for small molecule structure ID

Sympatec GmbH System-Partikel-Technik WINDOX 4. Electronic Records/ Electronic Signatures Compliance Assessment Worksheet for 21 CFR Part 11

Spectroscopy Configuration Manager (SCM) Software. 21 CFR Part 11 Compliance Booklet

TIBCO Spotfire and S+ Product Family

Achieving 21 CFR Part 11 Compliance with Appian

Considerations for validating SDS Software v2.x Enterprise Edition for the 7900HT Fast Real-Time PCR System per the GAMP 5 guide

Supplement to the Guidance for Electronic Data Capture in Clinical Trials

Thermo Scientific icap 7000 Series ICP-OES. Low cost ICP-OES analysis high quality data

Using Chromeleon Chromatography Management Software to Comply with 21 CFR Part 11

REGULATIONS COMPLIANCE ASSESSMENT

SIMATIC SIMATIC PCS 7 V8.0. Electronic Records / Electronic Signatures. Compliance Response. Answers for industry.

Third Party Instrument Control with Chromeleon Chromatography Data System (CDS) Software

CoSign for 21CFR Part 11 Compliance

A fully quantitative research method for the analysis of lead in whole blood using the Thermo Scientific icap Q ICP-MS

Quantum View Manage Administration Guide

TargetQuan 3 Software. Leading the way in regulatory. POPs quantification. Bullet Bullet Bullet

Manual 074 Electronic Records and Electronic Signatures 1. Purpose

Quantum View SM Manage Administration Guide

Guidance for Industry. 21 CFR Part 11; Electronic Records; Electronic Signatures. Electronic Copies of Electronic Records

Guidance for Industry. 21 CFR Part 11; Electronic. Records; Electronic Signatures. Time Stamps

Quality Manual # QS MD Logistics, Inc. (Signed copy available upon request) Prepared by Robert Grange, Director Quality

Thermo Scientific Qtegra Intelligent Scientific Data Solution Software. Delivering quality. Driving productivity

Thermo Scientific LIFECYCLE Asset & Service Management for Healthcare

Hospital Certified Electronic Health Record (EHR) Technology Questionnaire

Electronic Citizen Identities and Strong Authentication

UNCITRAL legislative standards on electronic communications and electronic signatures: an introduction

A unique biometrics based identifier, such as a fingerprint, voice print, or a retinal scan; or

HIPAA Security. 4 Security Standards: Technical Safeguards. Security Topics

Guidance for Industry Computerized Systems Used in Clinical Investigations

Thermo Scientific PepFinder Software A New Paradigm for Peptide Mapping

U.S. FDA Title 21 CFR Part 11 Compliance Assessment of SAP Records Management

[NUGENESIS SAMPLE MANAGEMENT ] AMPLE IMPROVING LAB EFFICIENCY, ANAGEMENT ACCELERATING BUSINESS DECISIONS. bigstock.com $69

Report on Government Information Requests

Data Management and Good Clinical Practice Patrick Murphy, Research Informatics, Family Health International

Thermal Analysis. Subpart A General Provisions 11.1 Scope Implementation Definitions.

Neutralus Certification Practices Statement

Why Use Electronic Transactions Instead of Paper? Electronic Signatures, Identity Credentialing, Digital Timestamps and Content Authentication

Microsoft Voucher Ordering Processes

Eclipsys Sunrise Clinical Manager Enterprise Electronic Medical Record (SCM) and Title 21 Code of Federal Regulations Part 11 (21CFR11)

Electronic Prescribing of Controlled Substances: Establishing a Secure, Auditable Chain of Trust

January 30, 2014 Mortgagee Letter

Good Electronic Records Management (GERM) Using IBM Rational ClearCase and IBM Rational ClearQuest

LabChip GX/GXII with LabChip GxP Software

Configuring DHCP for ShoreTel IP Phones

Department of Veterans Affairs VA DIRECTIVE 6510 VA IDENTITY AND ACCESS MANAGEMENT

Transcription:

Thermo Scientific Qtegra Intelligent Scientific Data Solution (ISDS) Software for 21 CFR Part 11 Compliant Laboratories Technical Note 43106 Key Words Compliance, Electronic Records, 21 CFR Part 11 Goal Demonstrate the tool set provided in Qtegra ISDS for operation in 21 CFR Part 11 compliant laboratories. Introduction Part 11 of Title 21 of the Code of Federal Regulations; Electronic Records; Electronic Signatures (21 CFR Part 11) includes the United States federal guidelines for storage and protection of electronically stored data and the application of electronic signatures. These guidelines have been developed to ensure that electronic records are reliable, authentic and comprehensible. This document examines all sections of the code and describes how the Thermo Scientific Qtegra Intelligent Scientific Data Solution (ISDS) Software supports 21 CFR Part 11 compliant environments. The new Qtegra ISDS Software platform provides a wide range of features, which enable laboratories to operate within total FDA compliance. These features include audit trails, support for electronic signatures and tools for integrated data managements. Part 11 Electronic Records; Electronic Signatures Subpart B - Electronic Records 21 CFR Sec. 11.10 Description Comment Sec. 11.10 Controls for Closed Systems Part B of Electronic Records 11.10 (a) Validation of systems to ensure accuracy, reliability, consistent intended Thermo Scientific products are developed in accordance to an established New Product performance, and the ability to discern invalid or altered records. Development and Introduction process (NPDI). This provides a continuous phase/gate review. All documents are stored in Microsoft SharePoint and therefore subject to a complete history. All development items are tracked in a fully auditable database. Each item is linked to a test case and outcome. Qtegra ISDS Software is subjected to automated testing procedures including regression testing, followed by installation, functional, alpha and beta testing. All software releases are subject to full validation processes. 11.10 (b) The ability to generate accurate and complete copies of records in both Qtegra ISDS Software stores records in both native format and human, readable human readable and electronic form suitable for inspection, review, format. Electronic records can be printed. and copying by the agency. Persons should contact the agency if there are any questions regarding the ability of the agency to perform such a review and copying of the electronic records. 11.10 (c) Protection of records to enable their accurate and ready retrieval Qtegra ISDS Software has all the necessary functionality to provide safe and secure throughout the records retention period. processing. The software ensures total compliance with regulations and includes a compliance expert system with rules for password creation and user rights management. 11.10 (d) Limiting system access to authorized individuals. Each user must be assigned to a group with defined privileges. The user has only access permission to that group to which they have been assigned.

2 21 CFR Sec. 11.10 Description Comment Sec. 11.10 Controls for Closed Systems Part B of Electronic Records 11.10 (e) Use of secure, computer-generated, time-stamped audit trails to Complete histories of changes in records are available and can be independently record the date and time of operator entries and compared at any time, from version to version. Comments on the actions that create, modify, or delete electronic records. Record changes can also be manually inserted. In addition, all deletions, changes shall not obscure previously recorded information. Such amendments or moving of the record will be documented. Complete audit trail documentation shall be retained for a period at least as trails can be inspected and exported (see Figure 2). 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 Qtegra ISDS Software follows a clear, structured sequence of process, of steps and events, as appropriate. which ensures that the workflow is performed in the correct order. For example, it is not possible to store a document without user authentication and a reason entered for any amendments to the document. Another example is the forced protocol fidelity in the Sample List where the user must follow a defined number of sample for standardization of quality checks. 11.10 (g) Use of authority checks to ensure that only authorized individuals All users must log in into the system prior to accessing it with a unique can use the system, electronically sign a record, access the name and password combination. All subsequent changes in the operation or computer system input or output device, alter a system are marked with unique name. record, or perform the operation at hand. 11.10 (h) Use of device (e.g. terminal) checks to determine, as appropriate, Qtegra ISDS Software operates in remote mode via Windows the validity of the source of data input or operational instruction. message queues. This component is not subject to the same safety criteria as a direct log in to the system. It is expected to establish such a link in the same credentials. 11.10 (i) Determination that persons who develop, maintain, or use electronic This is the responsibility of the user and should be controlled by user record/electronic signature systems has the education, training, created procedures and documentation. and experience to perform their assigned tasks. 11.10 (j) The establishment of, and adherence to, written policies that hold This is the responsibility of the user and should be controlled by user individuals accountable and responsible for actions initiated under created procedures and documentation. their electronic signatures, in order to deter record and signature falsification. Sec. 11.30 Controls for Open Systems Comment 11.30 Person who use open systems to create, modify, maintain, or Records are subject to a 256-bit AES encryption and can only be transmit electronic records shall employ procedures and controls decrypted with Qtegra ISDS Software. 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.

3 Figure 1. Example of electronic signature and verification process. Sec. 11.50 Signature Forms Comment 11.50 (a) Signed electronic records shall contain information associated Users have the option to sign records electronically. The with signing that clearly indicates all of the following: electric signature is encrypted with a time stamp (1) The printed name of the signer; embedded in the record. See Figures 1 and 2. (2) The date and time when the signature was executed; (3) The meaning (such as review, approval, responsibility, or authorship) associated with the signature. 11.50 (b) The conditions in paragraph (a) (1-3) concepts described in this Electronic signatures are subject to the same version section shall be subject to the same controls as electronic records control as the record itself. Electronic signatures will be and as part of any human readable form of electronic recording displayed on screen and in print. should be included. Sec 11.70 Connection Signature/Document Comment Electronic signatures and handwritten signatures are the electronic record of a running analysis that should to ensure that the signatures do not cut, copied or otherwise transferred to falsify an electronic record by ordinary means. Subpart C - Electronic Signatures Sec. 11.100 Electronic Signatures Basic Requirement (a) Each electronic signature shall be unique to one individual and shall not be reused by, or reassigned to, anyone else. (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. (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, 12420 Parklawn Drive, RM 3007 Rockville, MD 20857. Electronic signatures are inextricably embedded in the encrypted file. The signature is uniquely qualified with the the document and has no relevance to other documents. In priniciple, electronic signatures are validated with digital certificates. The company can build its own infrastructure for assigning digital certificates or commercial vendors such as VeriSign, GlobalSign, Thawte and CAcert. Figure 2. Export of audit trail.

4 Figure 3. Access control editor. Sec. 11.200 Components for Electronic Signatures and Controls (a) Electronic signatures that are not based upon biometrics shall: (1) Employ at least two distinct identification components such as A combined user ID and password is required to log in into the an identification code and password. system. (i) When an individual executes a series of signings during a single, continuous period of controlled system access, the first 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. (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. (2) Be used only by their genuine owners. A combined user ID and password is required to log in into the system. The signature award is presented by the confirmation of the password. After logging out, the user is required to log back into the system with a combination of the user ID and password. (3) Be administered and executed to ensure that attempted use of The user ID and password must be kept confidential by the an individual s electronic signature by anyone other than its owner. User ID must be unique with only one user of each ID genuine owner requires collaboration of two or more individuals. allowed on the domain, as per Windows authentication and the system administrator settings. Users are instructed to change their password to one that is known only to them. (b) Electronic signatures based upon biometrics shall be designed to ensure that they cannot be used by anyone other than their genuine owners. Qtegra ISDS Software does not currently support biometric signatures.

Sec. 11.300 Components for Electronic Signatures and Controls 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: (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. (b) Ensuring that identification code and password issuances are periodically checked, recalled, or revised (e.g., to cover such events as password aging). (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. (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. The user ID and password must be unique. This is ensured by Microsoft Windows and the administrator. Qtegra ISDS Software uses the Windows domain controller for password control. The network administrator should ensure that the Windows domain controller is configured to ensure that this criteria is met. N/A All log in and log off attempts are documented. A report is generated if a failed log in attempt is made. Technical Note 43106 thermofisher.com/qtegra-isds 2016 Thermo Fisher Scientific Inc. All rights reserved. Windows and SharePoint are trademarks of Microsoft Corp. Thawte is a trademark of Thawte, Inc. GlobalSign is a trademark of GMO GlobalSign K.K. VeriSign is a trademark of VeriSign, Inc. All other trademarks are the property of Thermo Fisher Scientific and its subsidiaries. This information is presented as an example of the capabilities of Thermo Fisher Scientific products. It is not intended to encourage use of these products in any manners that might infringe the intellectual property rights of others. Specifications, terms and pricing are subject to change. Not all products are available in all countries. Please consult your local sales representative for details. Africa +43 1 333 50 34 0 Australia +61 3 9757 4300 Austria +43 810 282 206 Belgium +32 53 73 42 41 Canada +1 800 530 8447 China 800 810 5118 (free call domestic) 400 650 5118 TN43106-EN 0316S Denmark +45 70 23 62 60 Europe-Other +43 1 333 50 34 0 Finland +358 10 3292 200 France +33 1 60 92 48 00 Germany +49 6103 408 1014 India +91 22 6742 9494 Italy +39 02 950 591 Japan +81 45 453 9100 Korea +82 2 3420 8600 Latin America +1 561 688 8700 Middle East +43 1 333 50 34 0 Netherlands +31 76 579 55 55 New Zealand +64 9 980 6700 Norway +46 8 556 468 00 Russia/CIS +43 1 333 50 34 0 Singapore +65 6289 1190 Spain +34 914 845 965 Sweden +46 8 556 468 00 Switzerland +41 61 716 77 00 UK +44 1442 233555 USA +1 800 532 4752