Microsoft Gold-Certified Partner Status achieved by genae
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genae
Contract Research Organization
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About Us
genae is dedicated to value-driven science & technology for the medical industries and helps you in obtaining predictable outcomes, on time, and on budget.
Visit genae.com to learn more about the solutions we offer:
* Clinical Trial Management
* Regulatory & Safety Services
* Digital Health
Contact information:
Justitiestraat 6b
Antwerp 2018
Belgium
Tel: +32 (3) 290 03 06
info@genae.com
www.genae.com
White Papers
Press Releases
MedicSense Bought By genae
Experts in Value-driven Science & Technology for the Medical Industries, genae, announced the acquisition of MedicSense, a Clinical, Regulatory Affairs and Quality Assurance consultancy firm.
genae Buys Hilbert Paradox
genae, a global service provider for the medical industries, today announced the acquisition of Hilbert Paradox (HPX), a digital health data management platform.
genae Launches staicy
genae, a global service provider for the medical industries, today announced the launch of staicy, a data-driven health and research management platform.
genae Invests in Meditrix
genae is involved in the development and commercialization of medical devices that change medical practice.
Videos
Connect the Dots of your Health & Research Project with staicy | Webinar | 25 June 2018
Join this 30 min. webinar to learn how staicy, genae's digital health data management platform, connects the dots of your health & research project by managing, analyzing, correlating and integrating your data, all while keeping full control.
Let’s Get you Ready for your Clinical Trial | Webinar | 24 January 2018
Join genae’s Sr. Clinical Project Manager, Thelma Bueno, for a 30 min. webinar to gain insight on the most important steps in designing your clinical trial and increasing your chances of successfully launching your product.
Are You Prepared For The New EU Medical Device Regulation? | Webinar | 9 November 2017
Join genae’s regulatory expert, Mieke Roelants, Sr. Regulatory Affairs Manager, for this 30 min. webinar to better understand the changes that clinical affairs teams should prepare for now to be successful under the new EU Medical Device Regulation.
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