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 (Herring) Maher

Medical Device Guru,
Greenlight Guru

Randy Armstrong


Isabella Schmitt
Isabella Schmitt, MBA, RAC

VP Life Sciences Solutions

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.



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 to explore your next step in medical device development.

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