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

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Featured Capabilities:

Document Management Training Management Product Development Design Control Risk Management CAPA Management Audit 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 Product Add-Ons

Get a personalized demo of Greenlight Guru Clinical today.

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Ultimate Guide to Comparing Quality Management System Solutions

This eBook compares the best QMS software solutions to help medical device companies make an informed decision when investing in a quality management system.

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FREE LIVE WEBINAR
October 4, 2023 | 1:00 pm ET

Bridging the Gap Between Clinical Research, Quality Management, & Device Design 

In the interactive world of medical devices, disjointed processes between product design, clinical research, and quality management can hinder innovation, compromise patient safety, and delay your time to market.

During this session, we will explore how the seamless collaboration between CROs like Proxima, design-focused companies like Velentium, and a flexible eQMS such as Greenlight Guru leads to safer, more effective, patient-centric devices. 

Unravel the intricacies of MedTech collaboration, discover the strategies that champion innovation, and craft your blueprint for success. Dive into a dialogue that reshapes the future of medical device creation. 

Watch the webinar
3 Panelists (4)-1
Key Topics:
  • Navigating the intricacies of synchronized design, clinical research, and quality management
  • Real-world case studies
  • Overcoming barriers: Strategies to address challenges in integrating core processes 
  • Golden Triad: Regulatory compliance, patient safety, and market dominance
  • Q&A session with our panel of experts.
Who should attend? 
  • Regulatory Affairs Professionals & Management
  • Quality Professionals and Management
  • Medical Device Executives
  • Product Development Engineers and Management
 Register Now  

Hosted by

         Laura-Maher
Moderator:
Laura (Herring) Maher

Medical Device Guru,
Greenlight Guru
randy-armstrong
Presenter:
Randy Armstrong

CTO
Velentium
Isabella Schmitt
Presenter:
Isabella Schmitt, MBA, RAC

VP Life Sciences Solutions
Proxima
         1611279855041
Presenter:
Sara Adams

Medical Device Guru,
Greenlight Guru

Greenlight Guru logo

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.

5bb950ff02efe918655fdd27_Proxima Logo + Tag - Blue

About Proxima CRO

Proxima CRO works with emerging biotech and medical device companies across all phases of development. As a contract research organization, we organize our team in two distinct areas: early stage advisory consulting and all-inclusive clinical trial services. The service you need. The speed you want. The attention you deserve. 


- Early Consulting
- Regulatory Consulting & Communicating With FDA 
- Clinical Study Planning
- Study Execution 
- Reimbursement & Market Access 

 
Visit their website to learn more.

5e13b364c5e98c952a048b16_velentium

 

About Velentium

Velentium is a contract design and manufacturing firm specializing in the development,
production, and postmarket support of diagnostic and therapeutic active medical devices,
especially implantables and wearables for neuromodulation and other Class III indications.

Velentium’s core competencies include:
-Systems Engineering
-Electrical Design
-Mechanical Design
-Firmware Development
-Software & Mobile App Development
-Embedded Cybersecurity
-Human Factors; Usability
-Automated Test Systems
-CGMP Contract Manufacturing

Visit Velentium.com to explore your next step in medical device development.

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