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Compliance In Focus
Posted by John Lehmann on Fri, Sep 27, 2013

BioOhio’s Regulatory Forum

BioOhio’s Regulatory ForumIMARC Research will be participating in BioOhio’s Regulatory Forum on October 3rd from 9:00 a.m. – 5:30 p.m. BioOhio has partnered with REU Associates to discuss regulatory issues that impact Ohio’s medical products industry. 

• The 510(k) e-Copy submission program
• Clinical data for medical device submissions
• Clinical monitoring
• Effective corrective action processes
• Risk management
• Controlling subcontractors, and more.

The day will feature presentations by FDA and industry experts, as well as panel discussions for you to ask the experts your unanswered regulatory questions. The event will facilitate great industry and professional networking in addition to the valuable content presented.  IMARC’s Shawn Kennedy will participate on a panel discuss and talk about Risk-Based Monitoring.
Please take time to view the agenda or contact Jennifer Goldberg with questions. 

We hope to see you on October 3rd.

Photo Credit:patentboy

PSIDE Guide

 

Topics: Risk-Based Monitoring, Medical Device CRO, BioOhio, Regulatory Forum, IMARC Research

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