Greenlight Guru
Greenlight Guru is the #1 provider of modern cloud-based solutions for the MedTech industry, helping companies bring life-changing products to market faster, more efficiently, and with less risk.
Greenlight Guru’s MedTech Suite provides quality management, product development, and clinical data management solutions, along with high-quality training and education required to keep up with the rapidly changing industry regulations.
Trusted by over 1,100 medical device companies across the globe, Greenlight Guru has been named by G2 as the #1 Medical QMS Software and by the Inc Magazine as a Best Place to Work. For more information, visit www.greenlight.guru.
FDA's Proposed Wound Dressing Rule: Industry Impacts & Regulatory Insights
Клинические данные: ключ к внедрению на рынок
Говоря на языке IVD
Управление рисками в клинических исследованиях
Язык MedTech: пациент, клиент или партнер?
Риск регулирования в сфере медицинских технологий: как действовать в FDA во время приостановки ра...
Андрагогика в медицинских технологиях: почему принципы обучения взрослых превосходят традиционное...
Руководство по возмещению расходов на медицинское оборудование
Программное обеспечение как медицинское устройство: обеспечение вашего цифрового будущего
Передовой этап инноваций в области медицинских устройств: от идеи до рынка
MedTech Startup Survival Guide with Steve Bell
Inside the Investor's Mind: What VCs Look For in MedTech
Shifting Sands of SaMD Cybersecurity Regulations
Tips For Being Prepared Post-EUA (Emergency Use Authorization)
Bringing Medical Devices Into The Home
Management Responsibility: The most important part of a QMS
The Role of dFMEA in Risk Management for Medical Devices
CSA vs. CSV: Modern Validation for Modern MedTech
Understanding the ROI of an eQMS
FDA Guidance on Artificial Intelligence (AI) in Medical Devices
The Right Way to Start a QMS: When, How, & What
3P510k: What Is a 510k 3rd Party Review & What are the Benefits?
Exploring Breakthrough Device Designation
Accelerating SaMD Development in a Compliant Agile Way
Moving MedTech Forward - The Past, Present & Future of Greenlight Guru
UDI and EUDAMED: Past, Present and Future State
Understanding LDTs & the FDA Proposed Ruling
Planning an FDA Submission
Recent FDA Draft Guidances
Becoming an Advisor to a Medical Device Company