Sterilization Validation & Monitoring System Based on NLPButton Technology Application for Steam Sterilization Presented by OPULUS 2006.

Slides:



Advertisements
Similar presentations
Micro Control Solutions Stability System II rev. 6.4
Advertisements

ILS Technology Named Top M2M Application Enablement Platform Vendor
Infrastructures For Information Inc. The Collaborative XML Content Company Content Company.
Radiopharmaceutical Production
Radiopharmaceutical Production
Stability Lab Information Manager Software by Stability Professionals, for Stability Professionals.
Copyright Hub Software Engineering Ltd 2010All rights reserved Hub Document Exchange Product Overview Secure Transmission for Transaction-based Documents.
OVERVIEW TEAM5 SOFTWARE The TEAM5 software manages personnel and test data for personal ESD grounding devices. Test and personnel data may be viewed/reported.
RF500 Wireless Monitoring  Exceptional data integrity  Complete peace of mind.
Cornerstone Base Station for Calibration Management Applied System Technologies, Inc N.W. 53rd Street, Suite 101 Fort Lauderdale, Florida
SAJAYA ® PARTNERSHIP… PARTNERING FOR SUCCESS. SAJAYA ® APPLICATIONS... SAJAYA ® is a new era in the world of software applications targeted for the Middle.
Audit of IT Systems SARQA / DKG Scandinavian Conference, October 2002, Copenhagen Sue Gregory.
Micro Control Solutions Annual Product Review rev. 6.5 “Click” for next slide Move to the next slide when the request appears.
CBER 1 Blood Establishment Computer Software (BECS) Michael Gorman, BA, MT(ASCP)SBB Consumer Safety Officer, CBER, OBRR, DBA September 15, 2009.
ETHYLENE OXIDE STERILIZATION VALIDATION
AFISS Prospectus of Services AFISS offers HACCP food safety and food quality systems development and management services including preparation for regulatory.
Security Controls – What Works
© 2004 Visible Systems Corporation. All rights reserved. 1 (800) 6VISIBLE Holistic View of the Enterprise Business Development Operations.
How ISO Standards Relates to Usability:. INTRODUCTION/ Before we can relate the ISO standards to usability, first we need to know what the meaning of.
An essential safety training tool for the modern world.
Selecting and Implementing an LMS for your Company Session Code #2411.
The Premier Software Usage Analysis and Reporting Toolset Maximizing Value for Software Users.
Laboratory Information Management Systems (LIMS) Lindy A. Brigham Div of Plant Pathology and Microbiology Department of Plant Sciences PLS 595D Regulatory.
Solution scenario Validated Pharmaceutical plant
Geosoft Systems Ltd. KITARON ERP&MES WISE MANAGEMENT
ShockWatch Cold Chain Services Portfolio Overview.
Presented to: Name of Customer Enhanced MET ONE 3400 Series Portable Airborne Particle Counters.
Rodney Mullins, Manufacturing Consultant InSource Software Solutions Business Center Drive Richmond, VA (804) MES “Unlocking The Value.
What is the It is the Next Generation, Calibration Station for the GasBadge ® Plus Personal Monitor
MethodGXP The Solution for the Confusion.
ArtClinica Address: 1175 Marlkress Rd, #2632, Cherry Hill, NJ 08034, USAPhone: Fax: ARTClinica.
Don Von Dollen Senior Program Manager, Data Integration & Communications Grid Interop December 4, 2012 A Utility Standards and Technology Adoption Framework.
Planning in production systems MES systems Slovak University of Technology Faculty of Material Science and Technology in Trnava.
 Maintains the Instrument Database  Generates the Calibration Schedules  Maintains Calibration Records  Provides Facility to enter All types of.
® Features and Benefits V3.1. TurboTag ® Features Temperature logger size of credit card Uses RFID reading protocols with EPC product codes More accurate.
Product Development Chapter 6. Definitions needed: Verification: The process of evaluating compliance to regulations, standards, or specifications.
InstantGMP: Electronic Batch Records System for GMP Manufacturing InstantGMP™ Inventory Control Module for GMP Manufacturing.
ICT Standards and Guidelines The Structure of the Project Akram Najjar CNSI – Senior Consultant Director of InfoConsult.
UL UK – European Affiliates Briefing – 6 July July 2004  The High Performance Organisation Group Ltd Online Auditing European Affiliates Briefing.
PwC 21 CFR Part 11 – A Risk Management Perspective Patrick D. Roche 07 March 2003, Washington D.C.
AREVA T&D Security Focus Group - 09/14/091 Security Focus Group A Vendor & Customer Collaboration EMS Users Conference September 14, 2009 Rich White AREVA.
An application architecture specifies the technologies to be used to implement one or more (and possibly all) information systems in terms of DATA, PROCESS,
The IT Quality Assurance FDA Validation Specialists Phone: 877-MGD-TEST ( ) n n n n Web Site:
Docking Stations The Future of Gas Detection. Goals for Today Increase your understanding of the capabilities and functions of Industrial Scientific Docking.
Archival Workshop on Ingest, Identification, and Certification Standards Certification (Best Practices) Checklist Does the archive have a written plan.
1 Hach Water Information Management Solution TM (Hach WIMS TM ) Overview.
1 1 Based on ISO 9000 accredited procedures Available to AAA financial members Registration completed and fee paid to AAA Must hold copy of the AAA manual.
CTD Dossier Preparation K. Srikantha Reddy Sr
The world leader in serving science Validation and Qualification Overview Mike Garry Software Product Manager Spectroscopy Software Platform Team.
Chapter 12 The Network Development Life Cycle
CABLING SYSTEM WARRANTY REGISTRATION. PURPOSE OF CABLING REGISTRATION.
GOOD DOCUMENTATION PRACTICES (GDP)
InstantGMP™ MD Electronic Device History File Software for Manufacturing Medical Devices.
의료용 S/W 기술문서 심사 방법 원 찬 요 유엘 코리아 발표자 소개 년 2 월 한양대 전자공 졸업 ~ : ㈜ 금성사 ( 현 LG 전자 ) 연구원 ~ : ㈜ 메디슨 규격팀 팀장
Energy Management System (EnMS) Standard Certification Documentation Kit.
The Traceability of Conductivity Meter and Cell Calibration in the Low Conductivity Ranges Jun Bautista, Director, Genzyme Metrology Genzyme Corporation,
Information day on EUROCONTROL Guidance Material on the application of Common Requirements for Service Provision  Aeronautical Information Services Provider.
November 6, 2013 Purchasing Controls & Supplier Quality Best Practices Beyond Compliance for the Medical Device Industry AdvaMed 2013 Bernie Liebler Technology.
© Akaza Research, LLC : 1 :: 10 Professional open source for clinical research.
Maintenance Management Software SPUDWEB TECHNOLOGIES PRIVATE LIMITED SPUMAINT Presented By :-
The staff at InstantGMP prepared the GMP for Dietary Supplements Compliance Series of presentations to focus on good manufacturing practices and GMP compliance.
Gesamtlayout der Wand Packaging 4.0 – intelligent, intuitive, integrated. TURBOCLEAN Packaging 4.0 Features FILMEX II with Film Performance Monitor.
Document No: GSC-21_034 Source: ISO/TC 184/SC 4 Industrial data
Author: Nurul Azyyati Sabri
Cold Chain Monitoring.
Engineering Processes
PeopleSoft Grants Julie Gustafson Product Strategy Manager
Document No: GSC-21_034 Source: ISO/TC 184/SC 4 Industrial data
Engineering Processes
Radiopharmaceutical Production
Presentation transcript:

Sterilization Validation & Monitoring System Based on NLPButton Technology Application for Steam Sterilization Presented by OPULUS 2006

What is a NLPButton data-logger? Anatomy of NLPButton data-loggers (actual size) Thermochrons (temperature) Hygrochrons (temperature/humidity suitable for EO sterilization/Intrinsically safe) Li-Battery Quartz clock Capacitive humidity sensor Microprocessor Humidity sensor inlet, covered by Gore-Tex

Content Steam Sterilization Validation & Monitoring System Components Regulatory Considerations Major Performance Characteristics Critical Functional Characteristics Documentation Requirements Support & Maintenance Cost of Ownership Benefits to the User

Steam Sterilization Validation & Monitoring System Components Thermochron data-logger Certificate of Calibration Docking Station for Programming/Data download Integrating Software SOP (Standard Operating Procedure) SCORM Compatible Competency Training IQ-OQ-PQ protocol for compliance verification 21 CFR Part 11 protocol for compliance verification

Regulatory Considerations Compliance with US FDA Requirements: –21 CFR Part 11 Compliance: The Steam Sterilization Validation & Monitoring System is 21 CFR Part 11 Compliant –IQ-OQ-PQ Verification Protocols are Included –21 CFR Part 11 Verification Protocols are Included –SOP (Standard Operating Procedure) are Included –SOP Competency Training: Web-enabled SCORM (DoD supported protocol) Compatible SOP Competency Training is Available –Complies with FDA’s “Guidance for the Industry for the Submission Documentation for Sterilization Process Validation in Application for Human and Veterinary Drug Products" Calibration: each data-logger’s Calibration is Traceable to NIST Reference Standard

NLPButton-T Data-Logger

Major Performance Characteristics Docking Station for iButton Programming/Data download iButton docking station for parallel programming/data down-load of the data-logger is available in various sizes to hold 8, or 16, or 32, or 50, or 100 iButtons The iButtons can be chained through a single Batch No. of multiple docking stations for parallel programming of 1,000’s of iButtons RS232, USB, & parallel interfaces are supported

Critical Functional Characteristics Sterilization Validation, Control, & Management Database setup –Applicable SOP –Sterilizer Dimensions –Specification limits –Bioburden limits –Cycle events –Area classification (e.g., ISO )

Critical Functional Characteristics Data-Logger Control & Management Data-logger Management –SOP assignment –Specification data –Automatic registration of logger events –Calibration specification –Calibration scheduling –Custom property option (e.g., BI application) –Sensor integrity verification –Attrition verification & optimization

Critical Functional Characteristics Cycle Specification with Load Assignment Cycle Specification

Critical Functional Characteristics Logger Positional Assignment Logger Positional Specifiation

Critical Functional Characteristics Logging Data Security

Documentation Requirements Summary of The Results

Documentation Requirements SQC/SPC

Documentation Requirements Temperature Control Chart Characteristics Including Load Analysis in Selected Sterilizer

Documentation Requirements Pareto Analysis of Measurement Distribution of The Sensors According to 3D Positions

Support & Maintenance 24/7 On-line Web Access for Interactive Support NIST Compliant Calibration Service IQ-OQ-PQ protocol verification –On-site or Web-supported 21 CFR Part 11 compliance verification –On-site or Web-supported via Intelligent Decision Tree SOP templates – 24/7 On-line Web access SCORM – 24/7 On-line Web, desktop, or enterprise training

Benefits to the User Low Purchase Cost Best in Class Price to Performance Ratio Total Solution with Full Regulatory Compliance –Certificate of Calibration –SOP –SCORM Compatible Training –Complies with FDA’s “Guidance for the Industry for the Submission Documentation for Sterilization Process Validation in Application for Human and Veterinary Drug Products“ Ensures Best Sterilization Practices