Content tagged with Webinar

7 results

Connect the dots of your health & research project with staicy | Webinar | 25 June 2018

View this webinar to learn how staicy can integrate seamlessly your internal and external clinical applications and utilize her proprietary functionality to uniquely select geographical storage location for your data.


Are You Prepared For The EU Medical Device Regulation? | Webinar | 29 November 2018

The EU Medical Device Regulation (MDR) was officially passed in May 2017 and manufacturers have until 2020, to be fully compliant with all changes set forth within the new regulation. View this 30 min. webinar to better understand the changes that clinical teams should prepare for now to be successful under the new regulation.


edc2go webinar | 18 July 2016

The main goal of any EDC solution is to be secure, user friendly and customized to fit your specific trial. View this webinar and find out how easy it is to build an eCRF with edc2go.


Let's Get you Ready for your Clinical Trial | Webinar | EU perspective

Whether you are a first-time inventor or a large manufacturer, the thrill of bringing a medical device to market is both exhilarating and overwhelming. The development of a successful device not only requires optimized design efforts, but also clinical, regulatory & marketing expertise.


core lab tracker webinar | 18 November 2015

Need an efficient, secure solution to track and transfer large image data? Discover core lab tracker in this webinar and find out how this great tool works.


Let's Get you Ready for your Clinical Trial | Webinar | US perspective

Whether you are a first-time inventor or a large manufacturer, the thrill of bringing a medical device to market is both exhilarating and overwhelming. The development of a successful device not only requires optimized design efforts, but also clinical, regulatory & marketing expertise.


Webinars

genae is committed to providing the latest information and thought leadership across the industry. genae webinars provide insights and understanding regarding today’s clinical standards and tomorrow’s regulatory changes.