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Das MasterControl™-Ressourcencenter ist Ihre persönliche Quelle für Produktinformationen. Wählen Sie die Artikel aus, die Sie gerne erhalten möchten, und klicken Sie unten auf der Seite auf „Submit“. An welchen Ressourcen sind Sie interessiert?



Beratung
Beratung

Audit/Assessment: Quality Event Management (QEM)
MasterControl Quality and Compliance Consulting™ (QCC) Certification/Accreditation Assistance Services
MasterControl Quality and Compliance Consulting™ (QCC) New Product Development/Acceptance Services
MasterControl Quality and Compliance Consulting™ (QCC) Quality Management Systems (QMS) Services
MasterControl Quality and Compliance Consulting™ (QCC) Quality Process Training
MasterControl Quality and Compliance Consulting™ (QCC) Regulatory Acceptance/Compliance Services
MasterControl Quality and Compliance Consulting™ (QCC) Services Overview
MasterControl Quality and Compliance Consulting™ (QCC) Supply Chain Management Services
MasterControl Quality and Compliance Consulting™ (QCC) Validation Services
Workshop: Corrective Action/Preventive Action (CAPA), Advanced Problem Solving to Identify and Correct Root Cause
Workshop: Quality Event Management (QEM) and Corrective Action/Preventive Action (CAPA)
Workshop: Quality Management System (QMS) Root Cause Investigations



Broschüre
Broschüre

6 Gründe für die Automatisierung Ihres Batch Record-Systems



Demo Video
Wir bieten interaktive Demonstrationen und Online-Kundendemonstrationen der MasterControl-Suite von Qualitätsmanagement-Lösungen an. Laden Sie jetzt eine Demonstration herunter.

MasterControl Clinical Quality Management System (CQMS)
Übersicht über das MasterControl Qualitäts-Management-System (QMS)



E-Book

(E-Pub Version) Convergence of Compliance & Technology
Compliance and Technology: How to meet changing FDA expectations



Fallstudie
Die folgenden MasterControl-Kunden sind Beispiele dafür, wie MasterControl Unternehmen aus verschiedenen Branchen hilft, Qualitäts- und Zulassungsherausforderungen zu meistern. Klicken Sie auf den Eintrag, um eine kurze Beschreibung zu erhalten.

Actelion's Quatro System
Aplicare
ARUP Laboratories
Asymtek
Bio-Imaging
Ecolab’s MasterControl System Continues to Grow
EMD Chemicals
How Ash Stevens Inc. Boosted Its Equipment Calibration and Maintenance Compliance
Hu-Friedy
Iowa Blood
ITxM Marks 10-Year Milestone of MasterControl Usage
Mallinckrodt Baker
Megadyne Medical Products - Successful Regulatory Compliance
MicroMed Case Study
Namsa
On-Site Training Complements MD Anderson’s Implementation
Schiff Nutrition
Sorenson Medical
Stay InFront
Syncardia Systems
Teamwork Key to OPK Biotech’s Successful Implementation
Teva Pharmaceuticals
Unity Lab Services: Assurance of Current Content is Crucial to Success
User Acceptance is Key to GOLM’s Successful Implementation
Validation a Focal Point in LifeCenter Northwest’s Implementation
Vascutek
Weider Nutrition
Zarbee’s Naturals nutzt MasterControl Spark™



Firmenanalyse
Firmenanalyse

A Road Map for Addressing Quality and Manufacturing Challenges in Life Sciences (LNS Research)
Aberdeen: The Cost of Quality: a Study on Life Sciences
Achieving Quality Across the Global Manufacturing Network
Addressing Quality and Manufacturing Challenges in Life Sciences (LNS)
Closed Loop Quality Management: Connecting the Value Chain (LNS)
Risk Management: Best Practices for Medical Device Profitability



Freie Dokumentenvorlagen
Freie Dokumentenvorlagen

Basic Policy SOP Template (Word Document)
Basic Procedure SOP Template (Word Document)
Basic Work Instruction SOP Template (Word Document)
MasterControl TMF Checklist Template



Infografik
Infografik

Closed Loop Quality Management
Driving Collaborative Growth in Life Sciences (LNS)
ISO 9001 QMS Structure Diagram
We've Programmed in ROI



Interactive Graphic

9 Fallstricke, die während des Dokumentenlenkungsprozesses vermieden werden sollten
Evolution of a QMS



Poll Reports

Quality System Poll Results: How Do You Compare With Your Quality Peers?



Produktdatenblatt
Die folgenden Komponenten sind Datenblätter für die einzelnen Produkte in der MasterControl-Suite von Qualitätsmanagement-Softwarelösungen. Klicken Sie auf den Eintrag, um eine kurze Beschreibung zu erhalten.

Das Besondere an Validierungsdiensten und -lösungen von MasterControl
Die Validierungsstrategie und die Vorteile von MasterControl
MasterControl Accessibility Standards for Section 508 Compliance Product Data Sheet
MasterControl Accident/Injury™
MasterControl Advanced Packet Types™
MasterControl All Access Product Summary
MasterControl Analytics™
MasterControl API Toolkit: Integrate Your EQMS with Core Business Solutions
MasterControl API Toolkit™
MasterControl Audit
MasterControl Audit Essentials™
MasterControl Bill of Materials (BOM)
MasterControl Business Process Library™
MasterControl Café
MasterControl CAPA
MasterControl Change Control
MasterControl Classes™
MasterControl Clinical Quality (GCP) JumpStart
MasterControl Clinical Quality Management System (CQMS)™”
MasterControl Collaboration™
MasterControl Copies™
MasterControl Customer Complaints
MasterControl Custom-Fit
MasterControl Deviations
MasterControl DHF JumpStart
MasterControl Document Collections
MasterControl Document Connections™
MasterControl Documents
MasterControl Education Services – On Demand Training™
MasterControl Educational Services
MasterControl Electronic Batch Records™ (EBR)
MasterControl eMDR™
MasterControl Enterprise Business Units™
MasterControl Enterprise Integrations™
MasterControl Enterprise Quality Management Software (EQMS)
MasterControl Equipment Calibration™
MasterControl Equipment Maintenance™
MasterControl Escrow Program
MasterControl eTMF Manager™
MasterControl Event Analyzer
MasterControl Exams™
MasterControl Flexible Options - Licensing/Packaging/Installation/Scale
MasterControl Forms Quickview™
MasterControl GCP Studies™
MasterControl GCPDocs Express™
MasterControl GLP JumpStart™
MasterControl GLP Studies™
MasterControl GMP JumpStart
MasterControl Government Contract Vehicles
MasterControl Guest Connect™
MasterControl Hosted™
MasterControl HR Finance™
MasterControl Incident Reporting™
MasterControl JumpStarts and Reference Models Overview
MasterControl Mobile™
MasterControl MS Word Integration
MasterControl Multi-Language Translations
MasterControl New Implementation Subscription Services
MasterControl Nonconformance™
MasterControl Not-for-Profit Pricing
MasterControl Organizer Gateway™
MasterControl Outlook E-mail Integration™
MasterControl Out-of-Specification™
MasterControl PDF Publishing™
MasterControl PDM Connector for PTC's Pro/Intralink™
MasterControl PDM Connector for PTC's Windchill™
MasterControl PDM Connector for SolidWorks PDMWorks™
MasterControl PDM Connector for SolidWorks® Enterprise
MasterControl PDM Connectors™
MasterControl Pharma R&D JumpStart
MasterControl Portal™
MasterControl Process™
MasterControl Project Management Services
MasterControl Projects™
MasterControl Promotional Materials™
MasterControl PTC® PDM Connectors
MasterControl QE Audit
MasterControl QEM CAPA Workshop
MasterControl QMS and QEM Systems for ISO Guided Companies
MasterControl Recorded Online Training™
MasterControl Reference Model™ - EDM Jumpstart
MasterControl Reference Model™ - TMF Jumpstart
MasterControl Regulatory Suite™
MasterControl Risk
MasterControl Risk Analysis™
MasterControl ROI Worksheet - Calculate Your ROI
MasterControl Rules™
MasterControl SharePoint Connector™
MasterControl SolidWorks® PDM Connectors
Übersicht über MasterControl Solutions™
MasterControl Spark Implementation Schedule
MasterControl Spark Implementation Schedule for Regulated Companies
MasterControl Spark Produktüberblick
MasterControl Submissions Locker™
MasterControl Submissions Ready™
MasterControl Supplier
MasterControl Supplier Corrective Action Request (SCAR)™
MasterControl Supplier Deviation™
MasterControl Supplier Scorecard™
MasterControl Sysadmin Support
MasterControl Technical Account Manager (TAM) Program
MasterControl Training™
MasterControl Transfer OQ™
MasterControl Transfer Performance Qualification (TPQ)
MasterControl Validation Strategy and Advantages
MasterControl Variance™
MasterControl/Kofax Interface™
MasterControl/PleaseReview Collaboration
MasterControl™-Suite für Qualitätsmanagement
QMS MasterControl CAPA Workshop for ISO Guided Companies
QMS MasterControl Root Cause Investigations Workshop for ISO Guided Companies
Trial Site Workshop
UL Compliance to Performance Advisory Services Company Profile and Partner Strategy
UL Compliance to Performance Courses from MasterControl
Validierungsdienste und -lösungen



Sonstige Broschüren und Unterlagen

Brochure: Dealing with QMS Regret
Borschüre: Fühlen Sie sich durch das CAPA-Durcheinander verloren?
Brochure: MasterControl Audit™
Brochure: MasterControl Clinical Management Software
Brochure: MasterControl Food Safety Quality Management System
Brochure: MasterControl Risk™
Brochure: MasterControl Simplifies IT Management
Brochure: MasterControl Supplier™
Broschüre: MasterControl-Training immer griffbereit
Building QEM Process Forms? MasterControl’s Process Bundles Will Save You a Bunch
Abonnement für die kundenspezifische Prozesspflege
Dovel-MasterControl Government Contract Vehicles
Global Accounts Program
How to Save $100 Grand Per Year!
MasterControl 2010 Presentation Guide
MasterControl Blood, Biologics, and Clinical Laboratory Solutions
MasterControl Cloud
MasterControl Corporate Brochure
MasterControl EQMS - Für eine herausragende Benutzererfahrung
MasterControl Medical Device Solutions
MasterControl Pharmaceutical & Biotechnology Solutions
MasterControl Quality Management Workshops Course Guide
MasterControl Software Solutions Overview
MasterControl’s ROI: A system that pays you back!
Mehr Freiheit für Sie mit MasterControl Mobile ™
Take Shelter in MasterControl Hosted™
Die schlauen Führungskräfte



Q&A
Die folgenden Komponenten sind Dokumente über das Qualitätsmanagement, die Antworten auf wichtige FDA-, ISO- und spezifische Branchenfragen enthalten.

Antworten auf Ihre brennenden Fragen zu MasterControl
CAP Accreditation and Document Control
CDER Official Offers Tips on GMP Inspections
CGMPs (Current Good Manufacturing Practices, aktuelle gute Herstellungspraktiken) in der Pharmaindustrie im 21. Jahrhundert: Ein risikobasierter Ansatz
Compliance with 21 CFR 820 and ISO 13485 Using MasterControl
Compliance with FDA's Good Tissue Practices
DIN EN ISO 14971: Risikomanagement für Medizingerätehersteller COMPLIANCE ACCELERATED
FDA Medical Device Investigator Offers Insights on Inspection
FDA's Quality Systems Approach to Pharmaceutical CGMPs
Guidelines For The European Medical Device Vigilance System
LORENZ Life Sciences Group and MasterControl Technology Integration FAQ
MasterControl Version 11: Most Frequently Asked Questions Pertaining to Security
New ICH Q10 Harmonization Guidance for the Pharmaceutical Industry
Q&A: Effective Project Management Can Help Ensure Compliance
Risikomanagement für Pharmaunternehmen gemäß FDA-Richtlinie Q9
The CAPA Engine and Your QMS System - Is it Driving Your Company Forward?



Technical Papers
Die folgenden Dokumente sind Technical Papers für MasterControl-Produkte, die ausführliche Informationen zu den einzelnen Produkten enthalten. Klicken Sie auf den Eintrag, um eine kurze Beschreibung zu erhalten.

15 Fragen zur Vorbereitung der Integration mit MasterControl
MasterControl Version 11.6 Hardware/Software Recommendations



Toolkit

10 Free Resources to Boost Your Training Management System
11 Free Resources to Boost Your FDA Readiness
11 Free Resources to Boost Your Medical Device FDA Readiness
12 Free Resources to Boost Your Pharmaceutical FDA Readiness
12 Free Resources to Boost Your Supplier Management System
25 Free Resources to Boost Your Quality Management System
8 Free Resources to Boost Your Audit Management System
9 Free Resources to Boost Your CAPA Management System
9 Free Resources to Boost Your Document Control System
IT Toolkit for Implementing an EQMS
MasterControl ROI Toolkit for EQMS Implementation



Webinar
MasterControl bietet ergänzende Webseminare über Themen zu Qualitätskontrolle und verwandten Branchen an. Wählen Sie nachstehend die Webinars aus, die Sie anzeigen möchten, und klicken Sie anschließend unten auf der Seite auf die Schaltfläche „Einreichen“.

Allgemein


ISO 13485:2016 Part 2: Getting Ready for Change
Software as a Service (SaaS) - Is it Right for Your Company?



Verbesserung Ihrer Qualitätsprozesse


CAPA Part 3: Effectiveness Checking and Management Review
Automating and Integrating Employee Training Processes to Ensure Compliance
Best Practices in Post-Market Intelligence
CAPA Part 1: Improving CAPA Systems with a Closed-loop Methodology
CAPA Part 2: Taking Effective Action
Integrating ISO 14971 and ICH Q9 Into Your Quality System
ISO 9001:2015 Teil 1: Vorbereitung auf bevorstehende Änderungen
ISO 9001:2015 Teil 2: Überblick über die neue QMS-Struktur
ISO 9001:2015 Teil 3: Risikobasiertes Denken erfolgt von impliziten bis expliziten Fakten
MasterControl - Quality Audit Challenges and Solutions
Program for Simplifying and Authoring SOPs
Six Steps to Better Medical Device Labeling: Dividends with Dollar Signs
Streamlining SOP Document Systems
The Importance of Effective CAPA and Root Cause Analysis Processes



MasterControl 8.0


MasterControl-Partner/Integrationen


Integration of Lorenz docuBridge and MasterControl for Electronic Submissions
Managing Documents & Submissions Lifecycles with MasterControl and LORENZ Solutions
Regulated Product Submissions: Preparing for RPS & How will it impact my industry?
Using Document Templates to Accelerate Time to Submissions with MasterControl and Sage



Produktentwicklung und -fertigung


Effective Bill of Materials (BOM) Management
Verbesserung des Lieferantenmanagements
Problem Solving in the Lean Supply Chain
Project Management Challenges in Medical Device New Product Development
Simplifying Batch Record Documentation in Preparation for MES/EBR
Streamlining Batch Record Documentation System in the Life Science Industry



Einhaltung behördlicher Vorschriften


AberdeenGroup - The Cost of Quality: a Study on Life Sciences
Automating Quality Audits for Regulatory Compliance
FDA Just Left! Now What?
GAMP 5 - A Risk-based Approach to Compliant GxP Computerized Systems
ISO 13485:2016 Teil 1: Bereiten Sie sich auf Änderungen vor
Overview: Quality System Regulation (QSR)
The FDA Called! Now What?
Working on a Post-Inspection FDA Response



Kapitalrendite


The Power of an Integrated Quality Management System (47:47)

White Paper
MasterControl verfügt über eine Vielzahl von White Papers der Branche, die Sie bei Ihren Schulungs- und Forschungsanforderungen unterstützen. Klicken Sie auf den Eintrag, um eine kurze Beschreibung zu erhalten.

21 CFR Part 11 Risk of Non-compliance
21 CFR Part 11 Sind Sie gerüstet für eine Inspektion durch die FDA?
21 CFR Part 11 System Validation (Risk Management Plan)
21 CFR Part 11: MasterControl Product Positioning
5 Tips for Getting Executive Backing for a New or Expanded EQMS
5 Trends Medical Device Companies Can’t Afford to Ignore in 2016
5 Ways MasterControl Ensures System Compliance with 21 CFR Part 11
9 Fallstricke, die während des Dokumentenlenkungsprozesses vermieden werden sollten
Änderungssteuerung – Kontinuierliche Qualitätsverbesserung in FDA- und ISO-Umgebungen
Annex 11 and 21 CFR Part 11: Comparisons for International Compliance
Annex 11: Die neuen Erwartungen der EU im Hinblick auf regulierte computergestützte Systeme
Automating Electronic Engineering Change
Automating Quality Compliance and Business Process within the Food and Beverage Industry
Automating Training Control Processes
Automatisieren von Dokumentenlenkungsprozessen zur Erfüllung von FDA- und ISO-Anforderungen: Steigern der Effizienz, Sicherstellen von Compliance und Verbessern der Rentabilität
Benötigt Ihr CAPA-System eine CAPA? Automatisieren der Korrektur- und Vorbeugemaßnahmen in FDA-Umgebungen
Calibration Software: The Buck Starts at User Requirements
cGMP and ISO 13485 Integrated Quality Management System
Clinical CAPA: Embedding Quality into Clinical Research
Compliance and Traceability in Regulated Industries Benchmark Report
Contracting Organizations and the Need for Written Transfer Obligations and Quality Agreements
Cost of Inaction - Taking Quality Management Processes Digital
Debunking 5 Common Assumptions About Quality in Business and Life in General
Die fünf gröẞten Herausforderungen bei der Stucklistenverwaltung
DIN EN ISO 13485-Grundlagen
Drug and Device Accountability Act of 2008: How Execs can Avoid Jail Time
Effective Nonconformance Management Key to FDA and ISO Compliance
Engineering and Quality Teams in Medical Device Firms: Can We All Get Along?
Ensuring the Adequacy of the Informed Consent Process in GCP Regulated Environments
Erfüllung der ISO-Norm 9001: 2008 mit automatisierten Tools
eTMF Management Essentials
FDA Experts Offer Top Tips to Optimize Your eCTD Submission
FDA Guidance for Clinical Investigators, Sponsors and IRBs Regarding Adverse Event Reporting in GCP Regulated Environments
FDA Inspections of Clinical Investigators: Are You Ready?
Final FDA Rule on Dietary Supplements - 21 CFR Part 111
Five Pharma Trends that Will Have the Biggest Impact in 2017
Fünf Trends, die 2014 für einen Wandel in der Medizinproduktindustrie sorgen
Five Trends Transforming the Medical Device Industry in 2015
Foolproof Investigations: A Proven Approach for Root Cause Analysis in a Regulated Environment
GAMP®5: A Risk-based Approach to Compliant GxP Computerized Systems
Getting Less For Your Money Isn't Always A Bad Thing
How 21 CFR Part 111 Helps Dietary Supplement Companies
How Effective Document Management Helps Pharmaceutical Companies Accelerate Time to Market
How Effective Training Management Can Help You Prevent Quality Issues
How Medical Device Firms Can Adapt to New Excise Tax
How Quality and Compliance Can Help Reduce the Cost and Time Involved in Executing Clinical Trials
How Regulated Companies Can Improve the Contract Management Process to Increase Efficiency and Reduce Risks
How Regulated Companies Can Leverage Mobile Technologies
How Software Helps Pharma/Biotech Maximize Value of External Resources
How to Address the Top 6 Pains in DHF Management
How to Kick-Start Your CAPA Process
How to Successfully Complete an FDA Inspection
How to Use Risk-Based Monitoring and Clinical CAPA to Ensure Compliance
ICH Q10 - Pharmaceutical Quality Systems - 'An Opportunity for Us All'
ISO 13485 -- Wechseln? Muss ich das??
ISO 14000 Standards
ISO 15189 Standards: For Medical and Clinical Laboratories
ISO 17025: What it Means for You and Your Laboratory
ISO 9001-2000 Standards: Automating Quality Systems
Managing Change Control to Comply with FDA and EU Regulations
Managing CLIA Compliance Costs: 6 Mistakes Every Laboratory Should Avoid
MasterControl: What's the Return on Investment?
Multipurpose Tool v. Integrated Best-of-Breed Modules: What’s the Difference?
Noncompliance to FDA Quality Standards: What's the Risk to Executives?
Pragmatic Approach to Computer Systems Validation
Qualifying Clinical Site Personnel Using Embedded Automation
Qualitätsaudit – Ein Tool für kontinuierliche Verbesserung und Compliance
Reducing the Documentation Burden in FDA Design Control
Reklamationsbearbeitung als integraler Bestandteil der FDA- und ISO-Compliance
Sarbanes Oxley Compliance - Challenges and Solutions for Sustained Compliance
Sechs Wege zur Optimierung Ihres Qualitätsmanagementsystems und zur Sicherstellung von FDA- und ISOCompliance
Simplifying CAPA: Seven Steps
Six Corporate Oversights of Quality and Compliance Issues in Pharmaceutical Environments
Software Automation in the Blood and Biologics Industry
Softwaretrends in der Medizingeratebranche
SOP Management as a Compliance Tool in FDA and ISO Environments
Ten Most Common Reasons for FDA 483 Inspectional Observations in Pharmaceutical Environments
Ten Most Common Reasons for FDA 483 Observations and Warning Letter Citations in Medical Device Environments
Ten Signs Your CEO Still Has No Idea About ISO 9001 and Lean
The Challenges of Building an Effective Structure for Sponsor-CRO Partnership
The Future of the FDA: Operating in an Electronic World
The Importance of Effective Quality Management in Complying with the European Union's GMP Standards
The Pharmaceutical Industry's Transition to Electronic Processes
The Pros and Cons of Buying Vs. Building a Quality Management System
The Top 5 Benefits of Electronic GLP Audit Management
The Value of Studying and Utilizing FDA's QSIT Manual
Top 10 Best Practices for Building Forms
Top 3 Strategies for Complying with USP <795> & USP <797>
Top 5 Trends in the Medical Device Industry in 2017
Top 5 Trends in the Pharmaceutical Industry in 2015
Die fünf besten Möglichkeiten, wie Dokumenten-Automatisierung den finanzellen Erfolg in der Life-Science-Branche steigern kann
Was kostet es, kein EQMS zu haben?
Wege zu einer erfolgreichen Lieferantenverwaltung, einer hohen Produktsicherheit und einer vollstandigen Compliance
What the Food Safety Modernization Act (FSMA) Means to the Food and Beverage Industry
What the Revised European Union’s Annex 11 Means to Life Science Companies
Writing and Enforcing Your SOPs for GxP Compliance Success