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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

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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 ON-DEMAND WEBINAR

New Year, New Rules - what to expect from EUMDR in 2025

Kick off 2025 with the insights you need to stay ahead in the ever-evolving MedTech landscape. Join us for an exclusive session featuring regulatory expert Dr. Bassil Akra as we dive deep into critical updates and challenges impacting medical device companies under EUMDR.

Whether you’re preparing for your next audit, aligning your quality system with updated standards, or simply staying informed, this webinar will equip you with the knowledge and tools to thrive in a changing regulatory environment.

Specifically, this webinar will help you:
  • Get clarity on the anticipated updates and changes in EUMDR that will affect medical device businesses.
  • Identify the key obstacles companies face in 2025 and discover actionable solutions to overcome them.
  • Learn practical approaches to align your Quality Management System with updated regulatory requirements and audit expectations.
  • Explore opportunities that arise from proactive compliance and stay competitive in the evolving market.
  • Leverage firsthand expertise from a recognized authority in EUMDR policies to inform and enhance your regulatory strategy.

Watch the webinar
New Year, New Rules EUMDR 2025-2
Who should attend?
  • Quality Professionals and Management
  • Regulatory Affairs Professionals and Management
  • Clinical Professionals and Management
  • Medical Device Executives
  • Product Development Engineers and Management
Register Now  

Hosted by

Vernon-Baker
Moderator:
Vernon Baker

Sr. Medical Device Guru,
Greenlight Guru
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SPEAKER:
Dr. Bassil Akra

CEO and President
AKRA TEAM

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About Greenlight Guru

Greenlight Guru is the leading connected, cloud-based platform purpose-built for MedTech companies. The end-to-end solution streamlines product development, quality management, and clinical data management by integrating cross-functional teams, processes, and data throughout the entire product lifecycle.

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 Dr. Bassil Akra

Dr. Bassil Akra is CEO and President of AKRA TEAM in Germany (GmbH) and the USA (Inc), a globally acting consultancy company. Dr. Akra was the Vice President of Strategic Business Development at the Global Medical Health Services of TÜV SÜD Product Service GmbH. He has vast experience in leadership, business management, research, development, quality management, and regulatory approval of medical devices, combination devices, and ATMP Products.

Dr. Akra played an essential role during the implementation of the medical device regulation in Europe. He was also involved in the drafting of several European guidance documents (e.g. MEDDEV, MDCG, etc.) and International Standards. He spent the last years of his career at TÜV SÜD training and educating various stakeholders on EU Legislations. Dr. Akra is also member of the Board of the EU Association TEAM PRRC. He is also member of the MDR EY Survey Advisory Group.

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