Kivo launches unified DMS platform ‘Kivo GO’

Kivo’s expanded platform brings compliant collaboration and intelligent process automation to emerging Regulatory, Clinical and Quality teams

Kivo, the intuitive Document Management Solution for life sciences, introduced Kivo GO, a unified platform for emerging life sciences teams who need to work together efficiently across all functions while maintaining compliance and security.

"When it comes to advancing a new treatment, time to market is critical - both for the patients who need it and the company sponsoring it", says Kivo’s CEO, Toban Zolman. "However, these smaller Regulatory, Clinical and Quality teams often don’t have the budget or admin resources for an ‘enterprise’ solution - so they lose a shocking amount of time trying to manage documents and processes in a compliant way."

Kivo offers these teams a fit-for-purpose solution to accelerate their timelines with the launch of Kivo GO - a compliant collaboration solution with built-in modules for every function including RIM, eTMF, and QMS.

"We have been using the Kivo platform from the moment we needed a QMS and started our first regulatory submissions. Kivo was an easy choice and has proven to be the right choice." said Seppe De Gelas, Director of Regulatory Affairs and Quality Assurance at Hyloris Pharmaceuticals.

"Their intuitive interface has been adopted quickly by the entire development team - allowing both the CMC experts and the clinical team to seamlessly integrate internal documents, as well as controlled documents from external parties. Kivo allows the regulatory team to easily build submissions for different applications and regions, and now also provides training modules for our quality documents, and an eTMF module for our clinical trial management."