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I got it!


Mr David R Dills


David R. Dills, an independent Regulatory & Compliance Consultant with more than 22 years of hands-on experience and a proven track record within the FDA regulated industry, has an extensive regulatory and compliance background with Class I/II/III and IVD devices and managing and handling activities within the global regulatory and compliance landscape.

David R spoke at

Best Practices for FDA Inspection 2016 GlobalComplianc... Oct 2016
Seminar on What You Need to Do to Prepare for a Successful Inspection GlobalComplianc... Oct 2016
How FDA Trains Its Investigators to Review Sub-Systems for State of Co... GlobalComplianc... Aug 2016
Seminar on Complaint Handling and Management: From Receipt to Trending GlobalComplianc... Jul 2016
Conference on why FDA at my Facility is, and what do I do During an In... GlobalComplianc... Jul 2016
Seminar on Why is FDA at my Facility, and what do I do During an Inspe... GlobalComplianc... Jul 2016
How FDA Trains Its Investigators to Review Sub-Systems for State of Co... GlobalComplianc... Jun 2016
Seminar on Key Factors to Write an Effective Standard Operating Proced... GlobalComplianc... May 2016
Seminar on How FDA Trains Its Investigators to Review Sub-Systems for ... GlobalComplianc... Mar 2016
Maintaining an Effective CAPA Program and Using Risk Assessment Tools. AtoZ Compliance Mar 2016
FDA's 2011 Guidance on Financial Disclosure by Clinical Investigators Compliance Glob... Feb 2016
Boston Seminar on Surviving an FDA Inspection: Understand the Do's and... GlobalComplianc... Dec 2015
Importing and Exporting Medical Devices: A Primer on Regulatory Strate... NetZealous May 2015
2-day In-person Seminar on Effective Complaint GlobalComplianc... Jul 2013
Managing the IDE Investigational Device Exemption GlobalComplianc... Jun 2013
Medical Device Postmarketing Vigilance Reporting GlobalComplianc... May 2013
Effective Complaint Handling, Medical Device GlobalComplianc... Apr 2013
Managing Your Medical Device Reporting GlobalComplianc... Mar 2013

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