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More than a Quality Management System: Tools for the entire MedTech Lifecycle.

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Featured Capabilities:

Document Management Product Development Design Control Risk Solutions Training Management CAPA Management

Experience the #1 QMS software for medical device companies first-hand. Click through an interactive demo.

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Data collection and management designed for MedTech clinical trials.

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Featured Capabilities:

Electronic Data Capture (EDC) Electronic Case Report Forms (eCRF) Electronic Patient Reported Outcomes (ePRO) Ad-Hoc Data Collection (Cases) Post-Market Surveys

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Learn valuable, career-boosting skills for the Medical Device industry. Get access to hundreds of free resources as well as subscription-based courses and certifications.

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FREE ON-DEMAND WEBINAR
March 8, 2023

The Ugly Truth About Paper-Based QMS - Making the Switch to eQMS

MedTech companies face heavier regulation requirements than ever before, and an increasing need to ensure traceability within their system processes.

Yet, many companies have chosen to maintain their Quality Management System with antiquated documentation on paper, or in generic tools like Sharepoint, Google Docs, or Dropbox.

This outdated approach to a QMS is hard to manage, slows down the product development process, and creates massive inefficiencies within a company. Despite this, many companies are reluctant to make a change and modernize their QMS because it may seem too daunting.

This webinar will highlight why MedTech companies should be concerned about what tools they use to maintain traceability - from an economical, regulatory, and ethical standpoint, and how to make the switch to an eQMS without disrupting the current process.

Join us as we speak with several companies who have successfully migrated from paper to an eQMS. They will share their migration stories and the positive impact it has had on their business.

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Specifically, this webinar will help you:
  • Identify when you're ready to make the switch
  • Understand the impact an eQMS can have on speed and efficiency in your company
  • Learn how to prove the ROI of switching to your organization
  • Discover best practices for a successful eQMS implementation
Who should attend? 
  • Regulatory Affairs Professionals & Management 
  • Quality Professionals and Management 
  • Medical Device Executives 
  • Product Development Engineers and Management
  • Complaint and CAPA Management & Professionals 
 Register Now  

Hosted by

Etienne-Nichols-round
Presenter:
Etienne Nichols

Medical Device Guru and Community Manager,
Greenlight Guru

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Panelist:
Savanah Sitton

Director of Regulatory Affairs and Quality Assurance,
Milliken
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Panelist:
Alfonso Canto

QA Manager,
Tenacore
Amanda headshot
Panelist:
Amanda Feddersen

QA Manager,
Monitored Therapeutics, Inc.
Laura-Maher
Panelist:
Laura Maher

Medical Device Guru,
Greenlight Guru

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About Greenlight Guru

Greenlight Guru is the leading cloud-based platform purpose-built for MedTech companies. The end-to-end solution goes beyond traditional QMS needs by integrating cross-functional teams, processes, and data throughout the entire product lifecycle so device makers can proactively overcome execution gaps, streamline compliance, and accelerate market success. Greenlight Guru’s platform is used by organizations across the globe that are replacing their disjointed, legacy tools and solutions to bring life-changing products to people faster, and with less risk. Visit our homepage to learn more.

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About Milliken & Company

Materials science expert Milliken & Company knows that a single molecule has the potential to change the world. With innovative solutions across the textile, flooring, specialty chemical, and healthcare industries, Milliken answers some of the world’s greatest challenges. Named to the World’s Most Ethical Companies list by Ethisphere Institute for 14 years, the company meets the moment with an unwavering commitment to delivering sustainable solutions for its customers and communities. Eight thousand associates across 46 locations globally rally behind a common purpose: to positively impact the world for generations.

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About Tenacore

Tenacore LLC is a healthcare technology management company providing clinical equipment lifecycle solutions to the global healthcare technology community through quality service delivery and dedication to continuous improvement. Specializing in the depot-based service and repair of a broad range of medical equipment, Tenacore's expansion across the United States paired with its multi-vendor service expertise and scalability uniquely positions the company to offer a cost effective and quality alternative to site-based service.

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About Monitored Therapeutics, Inc.

Monitored Therapeutics Inc. (MTI) is Remote Patient Monitoring Company focused on COPD, Asthma, Lung Transplant, and Cystic Fibrosis with four proprietary products - GoSpiro® Home Spirometer, GoHome™ Patient Health Monitor, GoClinic, GoECG and the MTI CarePortal™. MTI extends Access to Care to the patient and provider through a standardized platform, increasing Patient Engagement, Drug Adherence and Quality of Life while decreasing overall healthcare costs by keeping patients in their homes and out of the hospital.

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