FDAnews Announces — Centralized Submissions Management: Planning, Tracking, Resource Management and Metrics in Real Time Webinar, Sponsored by Sylogent, Dec. 1, 2016
Falls Church, VA (PRWEB) November 16, 2016 -- Centralized Submissions Management:
Planning, Tracking, Resource Management and Metrics in Real Time
Sponsored by Sylogent
**FDAnews Free Webinar**
Dec. 1, 2016 — 1:30 p.m. – 2:30 p.m. ET
http://info.fdanews.com/centralized-submissions-management
What do manufacturers have on their plates? Maybe, a little bit of alphabet soup?
Drugmakers have their INDs, NDAs, 505(b)(2)s.
Generics and orphan drugs have ANDAs.
And devicemakers have their 510(k)s, PMA, PDPs and de novo applications.
That’s a lot to keep up with. And the expectation is to do more with less. And that’s next to impossible.
Who wouldn’t like to get it right the first time? With no duplication? No repetition? No lost documents?
Join Jack Yeager founder of Sylogent on Dec. 1 when he’ll discuss software solutions that streamline and automate core business processes saving millions of dollars through improved compliance, reduced employee workload and lower operating costs.
Attendees will learn how Centralized Submission Management can benefit their organization including:
• Leveraging technology to help ensure submissions are completed on time, with minimal resource impact.
• Simplifying the submission process.
• Improving communications.
• Anticipating resource issues.
• Visualizing processes and issues.
Register today and discover the benefits of a centralized submission management system.
Meet the Presenter:
Jack Yeager, Founder of Sylogent
Jack Yeager has over 25 years experience working on process automation, including a patent in 2005. His experience spans a variety of industries including manufacturing, insurance, lending and life sciences. He formed Sylogent in 2008 to focus on compliance process automation that reduces the time, effort and cost to publish required information. Jack is currently focused on streamlining the complicated, but critical, submission process.
Who Will Benefit:
• Regulatory Managers
• Regulatory Affairs Specialist
• Project Managers
• Senior Management
• Clinical Operations
• QA/QC
• Legal
Webinar Details:
Centralized Submissions Management:
Planning, Tracking, Resource Management and Metrics in Real Time
Sponsored by Sylogent
**FDAnews Free Webinar**
Dec. 1, 2016 — 1:30 p.m. – 2:30 p.m. ET
http://info.fdanews.com/centralized-submissions-management
Easy Ways to Register:
Online: http://info.fdanews.com/centralized-submissions-management
By phone: 888-838-5578 or 703-538-7600
About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.
Michelle Butler, FDANEWS, http://www.fdanews.com, +1 (703) 538-7665, [email protected]
Share this article