For many MedTech companies, especially those that manufacture high-risk devices, clinical trials are a crucial part of getting medical devices to market and keeping them there. In fact, clinical activities, both pre-market and post-market, were some of the top business objectives that respondents to our 2024 State of the MedTech Industry Benchmark Report told us they were focused on this year ..read more

This episode of the Global Medical Device Podcast features a compelling conversation with Perry Parendo, a seasoned expert in product development and project management within the MedTech sector ..read more

If there is one universal truth in MedTech clinical trials, it is that your study will take more time than you allot for it initially. Everyone, and I mean everyone, underestimates the amount of time their clinical studies will take ..read more

Greenlight Guru Clinical's recent introduction of Custom Collaborator Roles provides vital support to the MedTech clinical study arena. This feature brings a targeted solution to the challenges of managing large, multi-site clinical trials and surveys, focusing on the intricate needs of user roles and permissions management across many users ..read more

This recognition underlines Greenlight Guru's commitment to innovation and customer-centric service in the MedTech industry ..read more

If there is one universal truth in MedTech clinical trials, it is that your study will take more time than you allot for it initially. Everyone, and I mean everyone, underestimates the amount of time their clinical studies will take ..read more

The premarket approval (PMA) process is the method FDA uses to evaluate the safety and effectiveness of Class III medical devices before they can be placed on the US market.  ..read more

In Greenlight Guru’s 2024 State of the MedTech Industry Report, respondents cited a number of common challenges related to training management, including ..read more

In this episode of the Global Medical Device Podcast, host Etienne Nichols sits down with Kim Kaplan from ISACA at the MD&M West trade show in Anaheim, California, to discuss the pivotal Voluntary Improvement Program (VIP ..read more

In this episode of the Global Medical Device Podcast, host Etienne Nichols is joined by Gary Saner, a seasoned expert in medical device Unique Device Identification (UDI) and regulatory compliance ..read more