SMART-TRIAL
Healthcare Software · Denmark · 11-50 Employees
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Overview
Headquarters
2l K. Christensens Vej, Aalborg SV, Nort...Phone Number
+45 29887329Website
www.smart-trial.comRevenue
<$5 MillionIndustry
ZI Rank: 1
Signal Type
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ZI Rank
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About SMART-TRIAL
Greenlight Guru Clinical (formerly SMART-TRIAL) offers a Quality Management System tailored for the MedTech industry, featuring tools for the entire product lifecycle. Specialized in data collection and management for clinical trials, it provides capabilities like Electronic Data Capture and Patient Reported Outcomes. Targeting medical device companies, it focuses on assisting in various initiatives such as migrating from paper, preparing for regulatory submissions, managing postmarket quality, and more.Explore more
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SMART-TRIAL Tech Stack
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SMART-TRIAL News & Media
SMART-TRIAL® Appoints Adam Steadman as Chief Commercial Officer - Americas and Asia
AALBORG, Denmark--(BUSINESS WIRE)--SMART-TRIAL, the industry leader in Data Acquisition & Management systems built specifically for Medical Device & Diagnostics clinical investigations and registries, announced today that Adam Steadman has joined the company as Chief Commercial Officer, Americas and Asia. Adam Steadman, an international MedTech expert, joins SMART-TRIAL from one of the world’s largest CROs where he was Global Head of Clinical Development for Medical Device and DiagnostiSMART-TRIAL's co-founder clears up myths about the GDPR to help MedTech companies with new MDR compliance
Jon I. Bergsteinsson, a MedTech expert and co-founder of SMART-TRIAL, will be debunking myths about the EU General Data Protection Regulation (GDPR) and Medical Device Clinical Trials at this year's MedTech Summit. Jon will present a new talk called “Common Pitfalls in Medical Device Studies - How to Mitigate and Prevent Them” which will be streamed live on Wednesday the 14th of October as a part of the Clinical Evaluations and Investigations conference stream. WithSMART-TRIAL is Looking for the Future Stars of MedTech
SMART-TRIAL announces the Future Stars of MedTech program to help early stage MedTech companies with clinical data collection and regulatory compliance. The program will equip participating companies with clinical data collection tools, professional services, networking and discount schemes to facilitate their clinical and regulatory pathway. The aim of the program is to level the playing field by giving the early stage innovators access to the same resources as their more established peers. WitSMART-TRIAL uplifting study safety reporting for MedTech
New SMART-TRIAL Adverse Event reporting capabilities helps medical device companies comply with international standards and regulations on safety reporting in clinical studies Aalborg, August 17, 2020 SMART-TRIAL has deployed a new global release of its software to enable MedTech clinical teams to comply with international standards on Adverse Event (AE) Reporting, such as the ISO14155 and the Medical Device Regulation. This move is the first by any Electronic Data Capture vendor to provid
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Greenlight Guru Clinical (formerly SMART-TRIAL) offers a Quality Management System tailored for the MedTech industry, featuring tools for the entire product lifecycle. Specialized in data collection and management for clinical trials, it provides capabilities like Electronic Data Capture and Patient Reported Outcomes. Targeting medical device compa... Read More
