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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
June 11, 2024

Strategies for Navigating the EU MDR Extension Deadlines

This webinar will explore the complexities of the Medical Device Regulation (MDR) journey by deep diving into its multifaceted challenges and emphasizing the pivotal year of 2024 for the Medtech industry.

Enrico Perfler, 1Med founder, will provide key considerations for the question on everyone's minds: is the EU market still the optimal first choice for Medtech companies? He will also offer strategic guidance on overcoming contemporary regulatory hurdles and insights into the state of the industry in relation to the extension deadlines.

Chris Rush, Solutions Engineer at Greenlight Guru, will discuss best practices to collect clinical data and the ways purpose-fit solutions can streamline the entire process.

By attending this webinar, you will acquire valuable insights into regulatory compliance, best practices for clinical data collection, market entry strategies, and the evolving MedTech regulatory landscape.

Watch for free
Strategies for Navigating the EU MDR Extension Deadlines
Specifically, this webinar will cover:
  • MDR: What a challenging journey
  • The importance of 2024 in Medtech
  • EU market as first choice?
  • How to navigate current and future regulatory challenges
  • Best practices for clinical data collection
Who should attend?
  • Clinical Affairs Professionals and Management
  • Clinical Operations Professionals and Management
  • Regulatory Professionals and Management
  • Medical Device Executives
Register Now  

Hosted by

Enrico-Perfler
Speaker:
ENRICO PERFLER

Founder,
1Med
Chris Rush headshot1
Speaker:
CHRIS RUSH

Solutions Engineer,
Greenlight Guru
Etienne-Nichols-round
Moderator:
ETIENNE NICHOLS

Medical Device Guru,
Greenlight Guru

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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 1Med

Founded in 2014, with headquarter in Agno, Switzerland, and employing 100+ professionals delivering operational support across the globe, 1MED Group’s mission is to support all the MedTech organizations in facing the complexity associated with the development of innovative medical devices in compliance with MDR and FDA regulation.

Such expertise includes the entire technology life cycle, from research and development, through commercialization, including advanced preclinical testing, quality management systems implementations, regulatory advice, clinical trials management and post marketing support across the medical device development continuum with a cross-functional approach which led to win the certification and certification maintenance of more than 500 different medical devices in the last few years.

Visit their website to learn more.

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