Reviewing the most significant changes affecting medical device standards and guidance documents Understanding the MDSAP (goals and strategy) Analyzing the MDSAP main differences with standard auditing Understanding grading of MDSAP non-conformances Assessing MDSAP Audit structure and reporting to regulators More than six Notified Bodies are in the Pilot Program, Office audits and witnessed audits are required (conducted by regulators) And Much More... Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900968SEMINAR?channel=mailer&camp=Seminar&AdGroup=allconferencealerts_MAY_2017_SEO

Date : 4th May 2017 to 5th May 2017

Place : United States, Boston, ma

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900968SEMINAR?channel=mailer&camp=Seminar&AdGroup=allconferencealerts_MAY_2017_SEO

Contact Person:Eevnt Manager

Description:

Reviewing the most significant changes affecting medical device standards and guidance documents Understanding the MDSAP (goals and strategy) Analyzing the MDSAP main differences with standard auditing Understanding grading of MDSAP non-conformances Assessing MDSAP Audit structure and reporting to regulators More than six Notified Bodies are in the Pilot Program, Office audits and witnessed audits are required (conducted by regulators) And Much More... Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900968SEMINAR?channel=mailer&camp=Seminar&AdGroup=allconferencealerts_MAY_2017_SEO

Reviewing the most significant changes affecting medical device standards and guidance documents Understanding the MDSAP (goals and strategy) Analyzing the MDSAP main differences with standard auditing Understanding grading of MDSAP non-conformances Assessing MDSAP Audit structure and reporting to regulators More than six Notified Bodies are in the Pilot Program, Office audits and witnessed audits are required (conducted by regulators) And Much More... Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900968SEMINAR?channel=mailer&camp=Seminar&AdGroup=allconferencealerts_MAY_2017_SEO will be held in Boston, ma,United States on date 2017-05-05

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Deadline for abstracts/proposals : 3rd May 2017

Keynote Speakers : David R. Dills, Global Regulatory Affairs & Compliance Consultant currently provides regulatory affairs and compliance consultative services for early-stage and established Class I/II/III device, IVD, biopharmaceutical, cosmetics and nutraceutical manufacturers on the global landscape, and has an accomplished record with more than 27 years of experience in the areas of Regulatory Affairs, Compliance and Quality Systems. He has been previously employed, with increasing responsibilities by dev

Conference Highlights :Clinical Research Associates Clinical Project Managers Regulatory Affairs Professionals Clinical Investigators and Clinical Research Regulatory Affairs Management Regulatory Affairs Specialists Regulatory Project Leads/SME's QA Auditors Supplier Auditors GxP Auditors Compliance Specialists Clinical Affairs Quality Manager Quality Assurance Production/Operations Consultants

Venue :Boston, MA, United States

Check the event website for more details.