Know more about Device Classification, Class I Medical Device, Class II Medical Device, IDE, Class III Medical Device, PMA filing, Combination Product and more.

Date : 1st June 2017 to 1st June 2017

Place : United States, Fremont

Website :http://onlinecompliancepanel.com/webinar/FDA-REGISTRATION-MEDICAL-DEVICE-IVD-PRODUCTS-508277/JUNE-2017-ES-ALLCONFERENCEALERT

Contact Person:OCP Panel

Description:

Know more about Device Classification, Class I Medical Device, Class II Medical Device, IDE, Class III Medical Device, PMA filing, Combination Product and more.

Know more about Device Classification, Class I Medical Device, Class II Medical Device, IDE, Class III Medical Device, PMA filing, Combination Product and more. will be held in Fremont,United States on date 2017-06-01

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Deadline for abstracts/proposals : 31st May 2017

Keynote Speakers : Charles H. Paul is the President of C. H. Paul Consulting, Inc. - a regulatory, Lean Manufacturing, training, and technical documentation consulting firm. Charles is a management consultant, instructional designer and regulatory consultant and has led C. H. Paul Consulting, Inc. since its inception over 25 years ago. He regularly consults with Fortune 500 pharmaceutical, medical device, and biotechnology firms assisting them in achieving human resource, regulatory, and operational excellence. He

Conference Highlights :The medical device submissions process in the US is a complex process. The regulations at times can be confusing and appear to be vague or contradictory. It is imperative to understand the similarities and differences in submissions approaches when formulating a marketing strategy for your medical device. Incorrect classification decisions for medical devices for example, can be costly and extend the submissions process far beyond what it should. Formulating a proper submissions strategy begins

Venue :United States

Check the event website for more details.