Ennov is pleased to announce that we will be exhibiting at the 2020 DIA Regulatory Submissions, Information and Document Management (RSIDM) Forum being held at the Bethesda North Marriott Hotel and Conference Center in North Bethesda, MD on February 10-12, 2020.
DIA’s RSIDM Forum brings together industry and regulatory stakeholders working across the scope of regulatory information to examine current data standards and requirements and effective regulatory information management approaches to align related systems.
On Tuesday, February 11 at 4:15 pm, Ennov’s Kristen Mandello, DVM will be delivering a presentation entitled “Automation, Efficiency, and Risk Mitigation in Regulatory Aggregate Report Writing” which discusses the benefits of automation in Pharmacovigilance aggregate report writing.
Be sure to stop by booth #203 to learn more about Ennov’s unified Regulatory software suite that covers Regulatory Document Management, Submission Publishing and Regulatory Information Management.
Ennov to Exhibit at the 2020 DIA Regulatory Submissions, Information and Document Management (RSIDM) Forum
January 7, 2020
About Ennov
Ennov provides a comprehensive software platform to manage the most demanding processes of life sciences organizations in a compliant and efficient way. With over 20 years of experience, Ennov’s cloud-based solutions cover Regulatory Affairs, Pharmacovigilance, Quality, Clinical, and Document Management. Dedicated to innovation and excellence, Ennov’s solutions are used by more than 450 Life Science companies and 500,000 users worldwide, helping them to bring their products to market faster while maintaining compliance with regulatory requirements.
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