PLM Software Systems

Choose the PLM System that Will Accelerate Your Time to Market

If you are a regulated company, you need PLM software that will support your product in every phase of its lifecycle. MasterControl All Access will increase efficiency and ensure compliance in managing a product throughout its lifecycle, from research and development to design, manufacturing, and servicing. When you choose MasterControl, you are choosing:

Watch Related Videos

Download Free Resources
Interactive and Live Demonstration: MasterControl Quality Management System (QMS) Overview
Product Data Sheet: MasterControl DHF JumpStart
Product Data Sheet: MasterControl Bill of Materials™ (BOM)
Product Data Sheet: MasterControl All Access Product Summary
White Paper: How to Address the Top 6 Pains in DHF Management
White Paper: ISO 13485 -- Change? Do I Have To??
White Paper: Ten Most Common Reasons for FDA 483 Observations and Warning Letter Citations in Medical Device Environments
White Paper: Software Trends in the Medical Device Industry
Webinar: ISO 13485:2016 Part 1: Getting Ready for Changes
Webinar: Project Management Challenges in Medical Device New Product Development

Use the PLM Software that Addresses Your Unique Needs

MasterControl All Access is an end-to-end solution for medical device firms, pharmaceutical companies, CROs, and other life science organizations and regulated companies. Investing in a robust PLM system is a crucial step you must take to speed up your time to market, as well as to ensure regulatory compliance.

Regulated companies like yours have unique needs and greater challenges compared with other types of companies. MasterControl product managers, industry veterans who have walked your shoes, designed All Access to address the risks of noncompliance.

With MasterControl's integrated solution, you will be able to:

  • Manage all product information throughout its lifecycle using a single and centralized web-based repository with 24/7 access for all authorized users.
  • Automate enterprisewide processes such as document control, training management, CAPA, change control, nonconformances, audit, and customer complaints.
  • Automate all activities related to each process, including task distribution and routing, tracking and follow-up, escalation, and approval
  • Connect all quality and other processes throughout a product's lifecycle under one scalable platform that can grow with your organization over the long haul,
  • Collaborate with different teams regardless of location in a virtual collaboration space. You will be able to give system access to external parties, such as consultants and suppliers, for collaboration purposes.
  • Manage your supplier process efficiently, including supplier qualification, vendor lists, supplier audits and re-certifications, and supplier deviations.
  • Facilitate regulatory compliance, including submissions to FDA, ISO certification audits, and submissions for the purpose of obtaining CE Mark.
  • Improve your risk management process with the right capabilities, including electronic workflows, risk assessment forms, and analytics and reporting tools. You can integrate risk management with your other quality processes.
  • Strengthen and streamline your Bill of Materials (BOM) management with a powerful revision control functionality that will ensure you are using the latest documents for all components in manufacturing.

Leverage the Expertise Trusted by Life Science Companies

"As for SynCardia and MicroMed, I honestly don't think they would be viable businesses today had it not been for MasterControl or something like MasterControl and I don't know that there is anything like MasterControl."

Rodger Ford, Former CEO, SynCardia and MicroMed Cardiovascular

Learn More about How to Address Your PLM Software Needs

To learn more about how MasterControl can help you address your PLM system needs,contact a MasterControl representative.