February, 6-8, – Mariott Hotel and Conference Center, Bethesda, MD, USA
Ennov, a Regulatory software vendor, exhibits its Regulatory Software Suite at the DIA Forum at the Mariott Hotel and Conference Center (Booth 307), set to begin on February 6th.
Ennov has a comprehensive PV suite for Human and Veterinary drugs, including a complete pharmacovigilance database and analytics solution.
In the DIA 2017 Forum, we will be sharing our IDMS Whitepaper and present our eCTD247 solution which enables you to publish PSUR in eCTD format, as mandated by the EMA since June 2016. eCTD247 enables you to submit your eCTD (or NeeS) dossier with the minimum effort and time. We will also be showing our RIM solution to meet your RA deadlines.
eCTD247 is the only online eCTD solution and
- Has a pricing based on the number of documents in your submissions
- Is very easy to use, with minimal training time to become efficient and start publishing and submitting your eCTD
As a specialist of eCTD, Ennov has devised the most practical and cost effective solution for submitting PSUR in eCTD or NeeS format.
DIA’s Regulatory Submissions, Information, and Document Management Forum is the leading forum covering EDM (Electronic Document Management), ERS (Electronic Regulatory Submissions), and RIM (Regulatory Information Management) which represent the end-to-end process of managing regulatory submissions and documents.
This serves as the premier place for the discussion of emerging operational standards, best practices, and the processes for submission, creation, and maximum use of regulatory information, including the technology and processes.
This year focuses on the discussion of emerging operational standards, best practices, and the processes for submission, creation, and maximum use of regulatory information.