1 / WHITE PAPER Assessment of Vaisala Veriteq vlog Validation System Compliance to 21 CFR Part 11 Requirements The 21 CFR Part 11 rule states that the FDA view is that the risks of falsification, misinterpretation, and change (without leaving evidence) within the GMP environment are higher with electronic records than paper records, and therefore specific controls are required. Vaisala system is a hybrid system that employs the use of both electronic records and signed paper records. The electronic records in the Veriteq system are controlled such that, once created, they cannot be modified. This unmodifiable nature of the electronic records allows them to be printed and signed with full assurance that they represent a true representation of collected data. This white paper is a clause-byclause analysis of the requirements of 21 CFR Part 11 and how the Vaisala system responds to and helps users meet these requirements. Subpart A - General Provisions Section 11.1 Scope (a) The regulations in this part set forth the criteria under which the agency considers electronic records, electronic signatures, and written signatures executed to electronic records to be trustworthy, reliable, and generally equivalent to paper records and handwritten signatures executed on paper. Note that although the Vaisala system complies with 21 CFR Part 11 requirements where applicable, ultimate responsibility for 21 CFR Part 11 rests with persons responsible for electronic record content, just as the responsibility for compliance with paper records requirements generally lies with those responsible for the record s content.
2 (b) (c) (d) (e) 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. 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, Electronic records that meet the requirements of this part may be used in lieu of paper records, in accordance with Sec. 11.2, unless paper records are specifically required. Computer systems (including hardware and software), controls, and attendant documentation maintained under this part shall be readily available for, and subject to, FDA inspection. The electronic records created by the Vaisala system are used to create signed paper records. The electronic records are not intended to form part of an FDA submission but, rather, must be archived to back up submitted data. Not applicable. The Vaisala system does not employ electronic signatures and, consequently, signed paper records are required. The electronic records generated by the Vaisala system must be backed up and maintained by the user. Vaisala maintains backward compatibility in its vlog software. Records created by older versions of vlog can be read by newer versions of the software. However, users may want to archive a copy of the version used to create the electronic records as a backup reference. Section 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. Users may decide to archive the Vaisala system s printed records using a PDF (Adobe Acrobat) printer system and, under such circumstances, the responsibility for maintaining the electronic signature system is the responsibility of the user. (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 No comment. electronic signatures and, consequently, relies on printed records that must be signed. However, the Vaisala system can print signed electronic records using a PDF printer (Adobe Acrobat) and, under such circumstances, the user is responsible for setting up and maintaining such a printing system.
3 Section 11.2 Implementation - continued (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 sent to the 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. No comment. Section 11.3 Definitions (a) The definitions and interpretations of terms contained in section No comment. 201 of the act apply to those terms when used in this part. (b) The following definitions of terms also apply to this part: No comment. (1) Act means the Federal Food, Drug, No comment. and Cosmetic Act (secs (21 U.S.C )). (2) Agency means the Food and Drug No comment. 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. Not applicable. (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. The Vaisala system is closed in that no access is permitted to alter the data on electronic records. electronic or digital signatures. Rather, the system outputs printed records which must be signed. electronic or digital signatures. Rather, the system outputs printed records which must be signed.
4 (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. electronic signatures. Rather, the system outputs printed records which must be signed. The Vaisala system requires that users employ handwritten signatures on printed graphs and documents. Vaisala's system is a closed system due to required security levels using Windows authentication. An audit trail documents all interactions with the Vaisala system. Subpart B Electronic Records Section Controls for closed systems (a) Validation of systems to ensure accuracy, reliability, consistent intended performance, and the ability to discern invalid or altered records. Although validation is a customer responsibility, Vaisala offers validation assistance in the form of Installation (IQ) and Operation Qualification (OQ) protocols. Computer files generated by the Vaisala system are in a proprietary (to Vaisala only) format 1 using a checksum technique to detect invalid or altered records. 1 The vlog data logger system utilizes distributed encryption to protect files from modification of any type. The Logger (.spl) files contain a 32 bit encryption key (4.3 Billion combinations). The Graph (.spg) files also contain a separate (and different) 32 bit encryption key. The Download password has a separate 160 bit key (1.46E+48 combinations). The Calibration data has a separate 96 bit key (7.92E+28 combinations) stored in the loggers itself. Also, the data is stored in the logger files and graph files as raw binary values - not in a human readable format. All of the keys must be correct before vlog will display VERIFIED and SECURE. See for more information.
5 Section Controls for closed systems - continued (b) (c) 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. Protection of records to enable their accurate and ready retrieval throughout the records retention period. Complete and accurate electronic copies of records are available by copying the raw data files or by setting up a PDF printer (requires Adobe Acrobat or similar) in order to export graphs in PDF format. Note that the Vaisala system is a hybrid system that generates electronic records that must be printed and signed. On the data logger, electronic data is held internally in nonvolatile EEPROM memory. Once data has left the data logger, the media it is stored on, the backup strategy, and retrieval procedures are the responsibility of the user. Note that the data on the logger is considered to be transient data and is thus excluded from 21 CFR Part 11. This is because although the data logger initially acquires the data, it only temporarily stores it before passing it onto a PC and a printer to complete the task. For reference, refer to Complying with 21 CFR Part 11, Electronic Records and Electronic Signatures; Appendix 4; Key Areas for Guidance; Section 4.5 Transient Data (published by ISPE and PDA, 2001). (d) Limiting system access to authorized individuals. There is no provision or system access for any users to modify electronic records. The Vaisala system provides access control using Windows authentication. (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. The Vaisala system is based on the creation of secure data logger files that cannot be modified (without rendering the files completely unusable). Because of the unmodifiable files, there are no operations that are possible to be performed on the electronic data logger record after, or during, file creation. A complete "audit trail" is available with a Vaisala Veriteq vlog/ VL data logger files. All data associated with the electronic data logging record is captured in the data logger file. This data includes: the time and date the file was created the ID of the creator of the file a description of the data logger file the serial and model number of the data logger the status of the logger file (secure and verified) when the logger was last calibrated who the logger was last calibrated by when the logger is next due for calibration Users cannot disable or modify the content or the way data is written to the electronic record nor can the information be edited or deleted any time during or after the record is created. In addition, any changes made to data logger operating parameters in the middle of a recording session results in the creation of a completely new electronic record. Data in the logger is cleared.
6 Section Controls for closed systems - continued (f) (g) (h) (i) (j) Use of operational system checks to enforce permitted sequencing of steps and events, as appropriate. 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. Use of device (e.g. terminal) checks to determine, as appropriate, the validity of the source of data input or operational instruction. Determination that persons who develop, maintain, or use electronic record/electronic signature systems have the education, training, and experience to perform their assigned tasks. 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 (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. The Vaisala system does not allow modification of electronic records under any circumstances or sequence of steps taken by the user. The Vaisala system does not allow modification of original electronic records by any individual, authorized or not. The Vaisala system follows a proprietary protocol for communicating with its data logger devices that serves to positively identify each device and determine whether the data from that device is valid or invalid. Training requirements are the responsibility of the user. electronic signatures. However, the user can print signed electronic records using a PDF printer (Adobe Acrobat) and, under such circumstances, the responsibility for managing and controlling such a system is the responsibility of the user. Operational procedures are the responsibility of the user.
7 Section 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 Sec , 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. The Vaisala system is a closed system in that data files, once created, cannot be modified under any circumstances. The audit trail captures all interactions with the Vaisala system including the clearing of a data logger. Section 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. In accordance with current good practice, the Vaisala system generates a unique checksum value, called a Logger File ID number, every time data is downloaded from a data logger. This number is then included and referenced in the following: Logger File Creation Reports Logger Files Graph files that contain inserted logger file data Tabular listings and printouts The method in which Logger File ID Numbers are generated ensures that it is virtually impossible (one chance in 4.3 billion 1 ) that any two logger files can have the same ID number. In addition, any alteration of the electronic record renders the file completely unusable. The combination of these two features provides the non-refutable link between the original electronic record and the printed and signed reports. All interaction with the Veriteq system is tracked in the audit trail.
8 Subpart C - Electronic Signatures The Vaisala validatable data logging system is a hybrid system that incorporates both electronic and paper records. Data is measured and recorded in electronic form then printed onto paper to form the permanent record. The electronic records cannot be modified without rendering the files completely unusable. Once a paper record has been generated, it would be subject to the audit trail requirements for equivalent paper records. For more information, visit or contact us at Ref. B211051EN-A Vaisala 2010 This material is subject to copyright protection, with all copyrights retained by Vaisala and its individual partners. All rights reserved. Any logos and/or product names are trademarks of Vaisala or its individual partners. The reproduction, transfer, distribution or storage of information contained in this brochure in any form without the prior written consent of Vaisala is strictly prohibited. All specifications technical included are subject to change without notice.
21 CFR PART 11 ELECTRONIC RECORDS, ELECTRONIC SIGNATURES Compliance of PLA 2.1 21.11.2013 21 CFR Part 11 Compliance PLA 2.1 SEC. 11.2 IMPLEMENTATION. (a) For records required to be maintained but not submitted
Self-Assessment of eresearch Compliance with 21 CFR Part 11, Electronic Record; Electronic Signatures Subpart A General Provisions Sec. 11.1 Scope. (a) The regulations in this part set forth the criteria
White Paper No 01 I December 2010 Implementation of 21 CFR Part 11 in the epmotion Software Electronic records and electronic signatures in the regulated environment of the pharmaceutical and medical device
InfinityQS SPC Quality System & FDA s 21 CFR Part 11 Requirements www.infinityqs.com Copyright InfinityQS International Table of Contents Overview... FDA s 21 CFR Part 11 Requirements... PART 11 ELECTRONIC
Implementation of 21CFR11 Features in Micromeritics Software Software ID PART 11 ELECTRONIC RECORDS; ELECTRONIC SIGNATURES Subpart A General Provisions Sec. 11.1 Scope. 11.2 Implementation. 11.3 Definitions.
rsdm and 21 CFR Part 11 Meeting the 21 CFR Part 11 Burden without Overburdening The right solutions for smaller biopharma. Nothing more. Nothing less. Prepared by: Ken VanLuvanee www.virtualregulatorysolutions.com
21 CFR Part 11 Implementation Spectrum ES INFRARED SPECTROSCOPY T E C H N I C A L N O T E Introduction Compliance with 21 CFR Part 11 is mandatory for pharmaceutical companies and their suppliers to sell
The Impact of 21 CFR Part 11 on Product Development Product development has become an increasingly critical factor in highly-regulated life sciences industries. Biotechnology, medical device, and pharmaceutical
21 CRF 11 Electronic Records and Signatures Implement best practices by using FileMaker Pro 7 as the backbone of your 21 CFR 11 compliant system. By Todd Duell What does Title 21 of the Code of Federal
White paper inforouter in the Life Sciences Industry: 21 CFR Part 11 Compliance Overview of 21 CFR Part 11 The final version of the 21 CFR Part 11 regulation released by the FDA in 1997 provides a framework
NucleoCounter NC-3000, NucleoView NC-3000 Software and Code of Federal Regulation 21 Part 11; Electronic Records, Electronic Signatures (21 CFR Part 11) A ChemoMetec A/S White Paper September 2013 ChemoMetec
FILEHOLD DOCUMENT MANAGEMENT SYSTEM 21 CFR PART 11 COMPLIANCE WHITE PAPER Copyright 2012 FileHold Systems Inc. All rights reserved. For further information about this manual or other FileHold Systems products,
21 CFR Part 11 Compliance Using STATISTICA Last Updated: April 2003 This document was updated to reflect the FDA s latest guidance (released February, 2003) and the withdrawal of previous guidance.! STATSOFT
Information INF13/147 EN ScreenMaster RVG200 Paperless recorder FDA-approved record keeping Measurement made easy Guidance on the use of the RVG200 paperless recorder for electronic record keeping in FDA-approved
Full Compliance for and EU Annex 11 With the regulation support of Contents 1. Introduction 2 2. The regulations 2 3. FDA 3 Subpart B Electronic records 3 Subpart C Electronic Signatures 9 4. EU GMP Annex
January 2013 Page 1 DeltaV Capabilities for Electronic Records Management This paper describes DeltaV s integrated solution for meeting FDA 21CFR Part 11 requirements in process automation applications
www.qadata.co.za Introduction FDA Title 21 CFR Part 11:Electronic Records; Electronic Signatures; Final Rule (1997) INITIAL REGULATION RELEASED High profile audit findings Industry complaints to wasting
Oracle WebCenter Content 21 CFR Part 11 Certification Kim Hutchings US Data Management Phone: 888-231-0816 Email: firstname.lastname@example.org Introduction In May 2011, US Data Management (USDM) was
September 2004 Page 1 An integrated solution for meeting FDA 21CFR Part 11 requirements in process automation applications using a configurable off-the-shelf (COTS) solution Emerson Process Management.
Software Manual Part IV: FDA 21 CFR part 11 Version 2.20 OPTIMA Software Manual Part IV: FDA 21 CFR part 11 BMG LABTECH This manual was designed to guide OPTIMA users through the software features related
Declaration of Conformity 21 CFR Part 11 SIMATIC WinCC flexible 2007 SIEMENS AG Industry Sector Industry Automation D-76181 Karlsruhe, Federal Republic of Germany E-mail: email@example.com Fax: +49
FDA 21 CFR Part 11 Electronic records and signatures solutions for the Life Sciences Industry The Rule 21 CFR Part 11 Handwritten signature means the scripted name or legal mark of an individual handwritten
W H I T E P A P E R POLICY ISSUES IN E-COMMERCE APPLICATIONS: ELECTRONIC RECORD AND SIGNATURE COMPLIANCE FDA 21 CFR 11 ALPHATRUST PRONTO ENTERPRISE PLATFORM This white paper is written for senior executives
The following document informs about the CFR 21 Part 11 compliance status of the PTZ 32 Software Package which is used to drive and control an automated Tablet Testing System Type WHT 3ME and a Multiple
Agilent MicroLab Software with Spectroscopy Configuration Manager and Spectroscopy Database Administrator (SCM/SDA) Compliance with 21 CFR Part 11 Introduction Part 11 in Title 21 of the Code of Federal
Gap Analysis - Checklist 21 CFR Part 11 Electronic Records & Signatures his document is a proposal and starting point only. he type and extent of documentation depends on the process environment. he proposed
Using the Thermo Scientific Dionex Chromeleon 7 Chromatography Data System (CDS) to Comply with 21 CFR Part 11 Compliance Guide Table of Contents Introduction... 3 PART 11 ELECTRONIC RECORDS; ELECTRONIC
Agilent UV-Visible ChemStation with Security Pack Compliance with 21 CFR Part 11 Introduction Part 11 in Title 21 of the Code of Federal Regulations includes the US Federal guidelines for storing and protecting
T E C H N I C A L P A P E R SolidWorks Enterprise PDM and FDA 21CFR Part 11 This Technical Paper discusses the technical solutions provided by SolidWorks Enterprise PDM to address the FDA 21 CFR Part 11
Meeting the FDA s Requirements for Electronic Records and Electronic Signatures (21 CFR Part 11) Executive Summary...3 Background...4 Internet Growth in the Pharmaceutical Industries...4 The Need for Security...4
Thermal Analysis 21 CFR 11 Compliance 21 CFR Part 11 Electronic Records; Electronic Signatures General concept The U.S. Federal Food and Drug Administration (FDA) has issued regulations that provide criteria
VISIONsecurity Software: 21 CFR Part 11 Compliance The information in this publication is provided for reference only. All information contained in this publication is believed to be correct and complete.
AutoSave Achieving Part 11 Compliance A White Paper Synopsis This whitepaper provides information related to FDA regulation 21 CFR Part 11 (Part 11) for organizations considering MDT software solutions.
Electronic Document and Record Compliance for the Life Sciences Kiran Thakrar, SoluSoft Inc. SoluSoft, Inc. 300 Willow Street South North Andover, MA 01845 Website: www.solu-soft.com Email: firstname.lastname@example.org
FUNCTIONAL REQUIREMENTS SPECIFICATION FOR THE EXAMPLE VALIDATION SPREADSHEET SERVING OFNI SYSTEMS RALEIGH, NORTH CAROLINA DOCUMENT NUMBER: FRS-001 DATE ISSUED: 11/12/08 REVISION: 0 PREPARED BY DANIEL WATERMAN
Technical Note 54 Using Chromeleon Chromatography Management Software to Comply with 21 CFR Part 11 The Electronic Records and Signatures Rule 1, known as 21 CFR Part 11, was established by the U.S. Food
Guidance for Industry 21 CFR Part 11; Electronic Records; Electronic Signatures Electronic Copies of Electronic Records Draft Guidance This guidance document is being distributed for comment purposes only.
in the BioPharma Industry White Paper v1.0 July 2005 I. Introduction...3 II. Overview of Regulations...3 III. Overview of Validation...4 a. Validation...4 b. Security s Part Within Validation...6 IV. Introduction
Draft Guidance for Industry -- Not For Implementation Guidance for Industry 21 CFR Part 11; Electronic Records; Electronic Signatures Maintenance of Electronic Records Draft Guidance This guidance document
Nova Southeastern University Standard Operating Procedure for GCP Title: Electronic Source Documents for Clinical Research Study Version # 1 SOP Number: OCR-RDM-006 Effective Date: August 2013 Page 1 of
Intland s Medical Template Traceability Browser Risk Management & FMEA Medical Wiki Supports compliance with IEC 62304, FDA Title 21 CFR Part 11, ISO 14971, IEC 60601 and more INTLAND codebeamer ALM is
Empower TM 2 Software 21 CFR PART 11 COMPLIANCE ASSESSMENT Revision A, December, 2005 1 of 14 Waters Corporation Note: Information presented in this document assumes that the appropriate Empower 2 System
Guidance for Industry 21 CFR Part 11; Electronic Records; Electronic Signatures Time Stamps Draft Guidance This guidance document is being distributed for comment purposes only. Comments and suggestions
Implementing CitectSCADA to meet the requirements of FDA 21 CFR Part 11 Version 2.0 July 2008 FDA 21 CFR Part 11 READY Reversed out on solid background colour Background In 1991, members of the pharmaceutical
Spectroscopy Configuration Manager (SCM) Software 21 CFR Part 11 Compliance Booklet Notices Agilent Technologies, Inc. 2015 No part of this manual may be reproduced in any form or by any means (including
Eclipsys Sunrise Clinical Manager Enterprise Electronic Medical Record (SCM) and Title 21 Code of Federal Regulations Part 11 (21CFR11) The title 21 code of federal regulations part 11 deals with an institutions
Guidance for Industry Part 11, Electronic Records; Electronic Signatures Scope and Application U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research
Deployment Guide 21 CFR Part 11 Deployment Guide for Authors: Invensys Operations Management and TSD (Total System Design, an Optimation Company) Table of Contents by Section 1 Before you Begin...............................................................................................
21 CFR Part 11 LIMS Requirements Electronic signatures and records Compiled by Perry W. Burton. Version 1.4, 8 Sept 2014 Table of contents 1. Purpose of this document 1 1.1 Notes to version 1.4 1 1.2 About
Data Management PACT Workshop: Design & Operation of GMP Cell Therapy Facilities April 10 th -11 th, 2007 Data Management Discuss Database Development Design Process Tips Data Normalization Reporting Ideas
A technical discussion of Good Electronic Records Management using Rational software from IBM 04/03 Good Electronic Records Management (GERM) Using IBM Rational ClearCase and IBM Rational ClearQuest Matthew
THE ROLE OF WATERS EMPOWER SOFTWARE IN ASSISTING IN 21 CFR PART 11 COMPLIANCE Waters Empower Software Seamlessly Manages Regulated Data to Aid in 21 CFR Part 11 Compliance Summary The objective of this
U.S. FDA TITLE 21 CFR PART 11 COMPLIANCE ASSESSMENT OF SAP LEARNING SOLUTION Disclaimer These materials are subject to change without notice. SAP AG s compliance analysis with respect to SAP software performance
Guidance for Industry Electronic Source Data in Clinical Investigations U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) Center for
Guidance for Industry Computerized Systems Used in Clinical Investigations U.S. Department of Health and Human Services Food and Drug Administration (FDA) Office of the Commissioner (OC) May 2007 Guidance
Guidance for Industry COMPUTERIZED SYSTEMS USED IN CLINICAL TRIALS U.S. Department of Health and Human Services Food and Drug Administration Center for Biologic Evaluation and Research (CBER) Center for
Why LabX balance fully supports FDA 21CFR Part 11 This article is intended to answer some frequently asked questions concerning the support of FDA 21 CFR Part 11 within LabX pro balance, the METTLER TOLEDO
ee ab. pblue n. ig. p. manual GxP oftware manual epblue GxP Software manual Software version 20.4.1 075 900.874 Copyright 2012 Eppendorf AG, Hamburg. No part of this publication may be reproduced without
Minnesota State Colleges and Universities System Procedures Chapter 5 Administration Procedures associated with Board Policy 5.22 5.25.1 Use of Electronic Part 1. Purpose. This procedure establishes requirements
ALIX is free software: you can redistribute it and/or modify it under the terms of the GNU General Public License as published by the Free Software Foundation. REGULATIONS COMPLIANCE ASSESSMENT BUSINESS
A White Paper from Zaizi Limited March 2013 Zaizi Ltd is registered in England and Wales with the registration number 6440931. The Registered Office is 222 Westbourne Studios, 242 Acklam Road, London W10
WHITE PAPER SDS Software v2.x Enterprise Edition Considerations for validating SDS Software v2.x Enterprise Edition for the 7900HT Fast Real-Time PCR System per the GAMP 5 guide This white paper describes
9 Things you need to know about Continuous Monitoring Systems in FDA-Regulated Environments If you work in a life science company or any company that is regulated by the FDA, you know that you will have
TECHNICAL MANUAL AuthentiMax Software for GloMax -Multi+ Instruc ons for use of Product E8946. TM403 Revised 9/13 AuthentiMax Software for GloMax -Multi+ All technical literature is available on the Internet
Guidance for Industry Electronic Source Data in Clinical Investigations DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Comments and suggestions regarding this draft
Guidance for electronic trial data capturing of clinical trials 1 st November, 2007 Japan Pharmaceutical Manufacturing Association pg. 1 Table of Contents 1. Background... 3 2. Purpose... 3 3. Scope...
Signature Authentication aka: How to stop chasing after your clinical staff for signatures Elizabeth Nista, CQIA The Written Signature as a Validation Tool Signature is a requirement of multiple accrediting
Achieving 21 CFR Part 11 Compliance with Appian Executive Summary Software performance in the life sciences industry has extremely high standards. The FDA and other regulatory bodies require software used
Auditing Chromatographic Electronic Data Jennifer Bravo, M.S. QA Manager Agilux Laboratories Outline Raw data paper or electronic record? Controls for electronic data Auditing electronic records Warning
Rackspace Archiving Compliance Overview Freedom Information Act Sunshine Laws The federal government and nearly all state governments have established Open Records laws. The purpose of these laws is to
INTRODUCTION This book offers a systematic, ten-step approach, from the decision to validate to the assessment of the validation outcome, for validating configurable off-the-shelf (COTS) computer software
C O M P L I A N C E G U I D E ELECTRONIC RECORD AND SIGNATURE COMPLIANCE NASD Rules 3010(d) and 3110(c)(1)(C) SEC Rule 17a-4 15 USC 7001 et. seq. (E-SIGN) ALPHATRUST PRONTO ENTERPRISE PLATFORM This compliance
Wingspan Technology Signature Requirements for the etmf A Regulatory and Technological Assessment Kathie Clark Director, Product Management Wingspan Technology 1 November 2012 Signature Requirements for