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Online Resources

We provide recorded and live, online demonstrations of the MasterControl suite of quality management solutions. Select the items you would like to receive, then click on the submit button at the bottom of the page.

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Interactive and Live Demonstrations - Download Now

We provide interactive and customer online demonstrations of the MasterControl suite of quality management solutions. Download one now.

MasterControl Clinical Quality Management System (CQMS)
MasterControl Quality Management System (QMS) Overview
View Blood & Biologics 3-Minute Demo (3:00)
View FDA 3-Minute Demo (3:00)
View ISO 3-Minute Demo (3:00)
View Medical Device 3-Minute Demo (3:00)
View Pharmaceutical 3-Minute Demo (3:00)
View QMS 3-Minute Video (3:00)

Live Online Demonstration Request:
Please call 800-825-9117, or click here to schedule a demonstration of the MasterControl integrated quality management suite. A MasterControl representative will then contact you to schedule an online demonstration.

Pre-Recorded Webinars

MasterControl provides complimentary Web-based seminars on issues relating to quality control and related industries. Select the webinars below that you would like to view, then click on the submit button at the bottom of the page.

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

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

Improving your Quality Processes
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 Part 1: Prepare for Impending Changes
ISO 9001:2015 Part 2: New QMS Structure Overview
ISO 9001:2015 Part 3: Risk-based Thinking Goes from Implicit to Explicit
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 Partners / Integrations
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

Product Development and Manufacturing
Effective Bill of Materials (BOM) Management
Improving Supplier Management
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

Regulatory Compliance
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 Part 1: Getting Ready for Changes
Overview: Quality System Regulation (QSR)
The FDA Called! Now What?
Working on a Post-Inspection FDA Response

Please check back often as new seminars will be added.

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